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Recalls in July 2018

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    TeaSource recalls Roasted Chestnut loose leaf tea

    The product may contain almonds, an allergen not declared on the label

    TeaSource of Roseville, Minn., is recalling Roasted Chestnut loose leaf tea that may contain almonds, an allergen not declared on the label.

    No illnesses have been reported to date.

    The recalled product was sold in the company's three retail stores in the Twin Cities region and elsewhere in the U.S. through web and mail order.

    It comes packed in metal foil pouch (either silver or black), with a TeaSource label identifying it as “Roasted Chestnut” in one of four sizes: 1-lb., 4-oz., 2-oz., or sample.

    What to do

    Customers who purchased the recalled product on or after June 18, 2018, should return it to the place of purchase for a full refund.

    Consumers with questions may contact TeaSource at (877) 768-7233.

    TeaSource of Roseville, Minn., is recalling Roasted Chestnut loose leaf tea that may contain almonds, an allergen not declared on the label.No illnesse...
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      Forest River recalls Wildwood and Salem recreational trailers

      The trailer brakes may not function properly

      Forest River is recalling 64 model year 2019 Forest River Wildwood and Salem recreational trailers.

      The break-away safety switch may have been improperly wired so that it is not connected to a constant power source, thereby possibly preventing the trailer brakes from automatically applying if the trailer were to separate from the tow vehicle.

      Failure of the trailer to brake when it becomes detached from the tow vehicle can increase the risk of a crash.

      What to do

      Forest River will notify owners, and dealers will install a new wiring harness, free of charge.

      The recall is expected to begin August 4, 2018.

      Owners may contact Forest River customer service at 1-574-534-4058. Forest River's number for this recall is 69-0764.

      Forest River is recalling 64 model year 2019 Forest River Wildwood and Salem recreational trailers.The break-away safety switch may have been improperl...
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      Suzuki recalls model year 2018 DR-Z400S and DR-Z400SM motorcycles

      The brake lamp may not illuminate properly

      Suzuki Motor of America is recalling 191 model year 2018 Suzuki DR-Z400S and DR-Z400SM motorcycles.

      During assembly the resin that fills the rear brake stop lamp switch may have adhered to the internal contacts, which can prevent the brake lamp from illuminating, increasing the risk of a crash.

      What to do

      Suzuki will notify owners, and dealers will install a new stop lamp switch assembly, free of charge.

      The recall began on July 16, 2018.

      Owners may contact Suzuki customer service at 1-800-934-0934. Suzuki's number for this recall is 2A84.

      Suzuki Motor of America is recalling 191 model year 2018 Suzuki DR-Z400S and DR-Z400SM motorcycles.During assembly the resin that fills the rear brake...
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      GiftTree recalls Sherman Candy Caramels

      The product may contain pecans, walnuts, almonds and/or peanuts, allergens not declared on the label

      GiftTree, a gift basket company based in Vancouver, Wash., is recalling 94,000 units of “Sherman Candy Caramels” sold online in several Gift Baskets.

      The product may contain pecans, walnuts, almonds and/or peanuts, allergens not declared on the label.

      The recalled product is sold in the Metropolitan Gourmet Gift Basket, Encore Gourmet Gift Basket, Champagne and Confections Gift, Toast of California Wine Basket, California Classic Gift Basket, The 5th Avenue Wine Gift Basket, Fit for Royalty Gourmet Basket, As Good As Gold Gift Basket, Sophisticated Gourmet Mailer, Fresh Fruit and Chocolate Keepsake Chest, Country Estate Gift Basket, Italian Roast Coffee Chest and Veuve Clicquot Tasting Gift Basket.

      The recalled “Sherman Candy Caramels” in gift baskets were shipped directly to consumers nationwide by Gift Services and sold by GiftTree and 1stopflorists.com from July 1, 2017, through July 16, 2018.

      What to do

      Customers who purchased or received gift baskets that contain the recalled product and have an allergy to pecans, walnuts, almonds or peanuts should not to consume, but dispose of the product.

      Consumers with questions or or who would like a replacement or credit towards future purchases may contact GiftTree’s customer relations department at (877) 657-7961 Monday through Friday, 5 a.m. – 4:30 p.m. (PST) or by email at recall@giftservices.com.

      GiftTree, a gift basket company based in Vancouver, Wash., is recalling 94,000 units of “Sherman Candy Caramels” sold online in several Gift Baskets.Th...
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      King Bio recalls Aquaflora Candida HP9, Lymph Detox, and Baby Teething liquids

      The products contain various microbial contaminants

      King Bio is recalling four lots of Aquaflora Candida HP9, Lymph Detox, and Baby Teething liquids.

      Inspection by the Food and Drug Administration found that the products contain microbial contaminants Pseudomonas Brenneri, Pseudomonas Fluroescens and Burkholderia Multivorans.

      The company says there have been no reports of injury or illness.

      Aquaflora HP9 product is used to control Candida, a fungal disease, while the Lymph Detox is for symptoms associated with lymphatic and Baby Teething liquids treat teething pain, irritated gums, delayed teething, etc.

      The following products, whose listed code dates are on the back of the packaging, are being recalled:

      Product;UPCLot #Exp.Distribution
      Aquaflora 
      Candida HP9 8
      oz. liquid in a 
      carton

      3-

      57955-

      80018

      -7

      1202-

      17R 


      1020-

      17C


      1010-

      17G 


      1114-

      17C

      12/02/19
      10/20/19
      10/10/19
      11/14/19
      8,000 bottles
      nationwide to 
      retail stores and 
      websites
      King Bio 
      Lymph Detox 
      2 oz. liquid in a 
      carton

      3-

      57955

      -50632

      -4

      0101-

      18BE

      01/01/20276 bottles 
      nationwide to 
      retail stores and 
      websites
      King Bio Baby 
      Teething 2 oz
      liquid in a
      carton

      0201

      18F

      13 bottles 
      marked NOT 
      FOR RESALE

      What to do

      King Bio is notifying its customers by letter and arranging for return and/or replacement. of all recalled products. Consumers who purchased the recalled products should stop using them and contact King Bio prior to returning them.

      Consumers with questions may contact King Bio at (866) 298-2740 Monday – Friday from 830am – 430pm (EST), or by e-mail at custcare1@kingbio.com.

      King Bio is recalling four lots of Aquaflora Candida HP9, Lymph Detox, and Baby Teething liquids.Inspection by the Food and Drug Administration found t...
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      Crate and Barrel Recalls Josephine floor mirrors

      The mirror’s glass can separate from the wooden backing and fall

      Crate and Barrel of Northbrook, Ill., is recalling about 830 Josephine floor mirrors.

      The mirror’s glass can separate from the wooden backing and fall, posing a laceration hazard.

      The company has received three reports of the mirror glass becoming loose or separating from the wooden backing. No injuries have been reported.

      This recall involves Crate and Barrel’s Josephine floor mirrors, sold individually or as a set of three mirrors that can be hung vertically or horizontally.

      The mirror consists of a larger rectangular mirror and a smaller square mirror on wooden backing that measures about 16 inches wide, three inches deep and 90.5 inches long.

      The hangtag that came with the mirror has the number 215-037 printed next to the bar code.

      The mirrors, manufactured in Mexico, were sold exclusively at Crate and Barrel stores nationwide and online at www.crateandbarrel.com from December 2016, through February 2018, for about $450 for a single mirror and $1,250 for a three-mirror set.

      What to do

      Consumers should immediately stop using the recalled mirrors and contact Crate and Barrel to arrange for a free replacement. Crate and Barrel is contacting all known purchasers directly.

      Consumers may contact Crate and Barrel at (800) 451-8217 from 7 a.m. and 9 p.m. (CT) Monday through Friday or online at www.crateandbarrel.com and click on “Product Recall” at the bottom of the page for more information.

      Crate and Barrel of Northbrook, Ill., is recalling about 830 Josephine floor mirrors.The mirror’s glass can separate from the wooden backing and fall,...
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      Major Pharmaceuticals recalls Valsartan

      The product contains a trace amount of an unexpected impurity

      Major Pharmaceuticals is recalling all lots Valsartan which was supplied by Teva Pharmaceuticals and labeled as Major Pharmaceuticals and is used to treat hypertension (high blood pressure) and heart failure.

      Trace amounts of an unexpected impurity -- N- nitrosodimethylamine (NDMA -- were found in an active pharmaceutical ingredient (API).

      NDMA has been classified as a probable human carcinogen as per International Agency for Research on Cancer (IARC) classification.

      The following product, distributed nationwide as unit dose blisters with 100 tablets per carton, is being recalled:

      Product DescriptionNDC NumberItem NumberLot NumberExpiration Date
      Valsartan 80mg Tablets, USP0904-6594-61302086T0179505/2019
      T0180705/2019
      T0171202/2019
      T0162502/2019
      T0159602/2019
      T0150002/2019
      T0146607/2018
      T0127007/2018
      Valsartan 160mg Tablets, USP00904-6595-61302087T0164605/2019
      T0178805/2019
      T0166805/2019
      T0152402/2019
      T0126907/2018

      What to do

      Consumers with questions regarding the recall may contact Major Pharmaceuticals customer support at (800) 616-2471, Option #1 Monday through Friday, 8 a.m. – 8 p.m. (EST).

      Major Pharmaceuticals is recalling all lots Valsartan which was supplied by Teva Pharmaceuticals and labeled as Major Pharmaceuticals and is used to treat...
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      Robert Bosch HDP5 High Pressure Fuel Pump Assemblies recalled

      Fuel may leak in the presence of an ignition source posing a fire risk

      Robert Bosch LLC has submitted a Defect Information Report based upon decisions made by Ford Motor Company and General Motors to conduct recalls to inspect and replace 6,493 Robert Bosch HDP5 High Pressure Fuel Pump Assemblies, part numbers 0261520518 and 0261520515.

      Welds between the pump housing and the mounting flange may fracture, possibly causing a fuel leak which, in the presence of an ignition source, can pose the risk of a fire.

      What to do

      Bosch is working with the affected vehicle manufacturers. Ford and GM will notify owners and dealers will replace the high pressure fuel pump assembly, free of charge.

      Owners may contact Ford customer service at 1-866-436-7332, Buick customer service 1-800-521-7300, Cadillac customer service 1-800-458-8006, Chevrolet customer service 1-800-222-1020, and GMC customer service at 1-800-462-8782.

      Robert Bosch LLC has submitted a Defect Information Report based upon decisions made by Ford Motor Company and General Motors to conduct recalls to inspect...
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      Model year 2019 Forest River Prime Time recreational trailers recalled

      The stove's propane supply line could fail

      Forest River is recalling 435 model year 2019 Forest River Prime Time recreational trailers.

      The stove is not isolated from the furnace return air, which potentially causes an inverted flame on the cooktop.

      The inverted stove top flame can cause the propane supply line to fail, increasing the risk of injury.

      What to do

      Forest River will notify owners, and dealers will install a panel to separate the stove top from the furnace return air feed, free of charge.

      The recall is expected to begin July 29, 2018.

      Owners may contact Forest River customer service at 1-574-862-3001. Forest River's number for this recall is 48-0755.

      Forest River is recalling 435 model year 2019 Forest River Prime Time recreational trailers.The stove is not isolated from the furnace return air, whic...
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      Teva recalls Valsartan and Valsartan Hydrochlorothiazide tablets

      The products contain a trace amount of an unexpected impurity

      Teva Pharmaceuticals USA is recalling 29 lots of single and 51 lots of combination valsartan medicines distributed under the Actavis label, which are used for the treatment of hypertension (high blood pressure) and heart failure.

      Trace amounts of an unexpected impurity -- N- nitrosodimethylamine (NDMA -- were found in an active pharmaceutical ingredient (API) manufactured by Zhejiang Huahai Pharmaceutical.

       NDMA has been classified as a probable human carcinogen as per International Agency for Research on Cancer (IARC) classification.

      Teva says it has not received any reports of adverse events related to this recall.

      The following products, packed in bottles and distributed nationwide, are being recalled:

      NDCProduct Description/Strength/Bottle SizeLotExpiration
      0591-2167-19Valsartan 40MG Tablets, USP 90 Count1196934MSep-2018
      0591-2167-19Valsartan 40MG Tablets, USP 90 Count1238462MMay-2019
      0591-2167-19Valsartan 40MG Tablets, USP 90 Count1268429AOct-2019
      0591-2167-30Valsartan 40MG Tablets, USP 30 Count1196936ASep-2018
      0591-2167-30Valsartan 40MG Tablets, USP 30 Count1238463AMay-2019
      0591-2167-30Valsartan 40MG Tablets, USP 30 Count1270617AOct-2019
      0591-2168-10Valsartan 80MG Tablets, USP 1000 Count1177114AJul-2018
      0591-2168-10Valsartan 80MG Tablets, USP 1000 Count1219360MFeb-2019
      0591-2168-10Valsartan 80MG Tablets, USP 1000 Count1250706AMay-2019
      0591-2168-19Valsartan 80MG Tablets, USP 90 Count1175947MJul-2018
      0591-2168-19Valsartan 80MG Tablets, USP 90 Count1175948MJul-2018
      0591-2168-19Valsartan 80MG Tablets, USP 90 Count1177115AJul-2018
      0591-2168-19Valsartan 80MG Tablets, USP 90 Count1219361AFeb-2019
      0591-2168-19Valsartan 80MG Tablets, USP 90 Count1240434MMay-2019
      0591-2168-19Valsartan 80MG Tablets, USP 90 Count1250704MMay-2019
      0591-2169-10Valsartan 160MG Tablets, USP 1000 Count1175922MJul-2018
      0591-2169-10Valsartan 160MG Tablets, USP 1000 Count1220826MFeb-2019
      0591-2169-10Valsartan 160MG Tablets, USP 1000 Count1236294MMay-2019
      0591-2169-10Valsartan 160MG Tablets, USP 1000 Count1240427MMay-2019
      0591-2169-10Valsartan 160MG Tablets, USP 1000 Count1270616AAug-2019
      0591-2169-19Valsartan 160MG Tablets, USP 90 Count1177880AJul-2018
      0591-2169-19Valsartan 160MG Tablets, USP 90 Count1220831AFeb-2019
      0591-2169-19Valsartan 160MG Tablets, USP 90 Count1263941AAug-2019
      0591-2170-05Valsartan 320MG Tablets, USP 500 Count1208000MOct-2018
      0591-2170-05Valsartan 320MG Tablets, USP 500 Count1208001MOct-2018
      0591-2170-05Valsartan 320MG Tablets, USP 500 Count1240425AJun-2019
      0591-2170-19Valsartan 320MG Tablets, USP 90 Count1208002AOct-2018
      0591-2170-19Valsartan 320MG Tablets, USP 90 Count1247282MMay-2019
      0591-2170-19Valsartan 320MG Tablets, USP 90 Count1263944MAug-2019
      0591-2315-19Valsartan and Hydrochlorothiazide 80/12.5MG Tablets, USP 90 Count1191191MAug-2018
      0591-2315-19Valsartan and Hydrochlorothiazide 80/12.5MG Tablets, USP 90 Count1191192MAug-2018
      0591-2315-19Valsartan and Hydrochlorothiazide 80/12.5MG Tablets, USP 90 Count1191193MAug-2018
      0591-2315-19Valsartan and Hydrochlorothiazide 80/12.5MG Tablets, USP 90 Count1191194MAug-2018
      0591-2315-19Valsartan and Hydrochlorothiazide 80/12.5MG Tablets, USP 90 Count1191195MAug-2018
      0591-2315-19Valsartan and Hydrochlorothiazide 80/12.5MG Tablets, USP 90 Count1238466MJun-2019
      0591-2315-19Valsartan and Hydrochlorothiazide 80/12.5MG Tablets, USP 90 Count1238467MJun-2019
      0591-2315-19Valsartan and Hydrochlorothiazide 80/12.5MG Tablets, USP 90 Count1253261MJul-2019
      0591-2315-19Valsartan and Hydrochlorothiazide 80/12.5MG Tablets, USP 90 Count1256125MJul-2019
      0591-2315-19Valsartan and Hydrochlorothiazide 80/12.5MG Tablets, USP 90 Count1277709MSep-2019
      0591-2316-19Valsartan and Hydrochlorothiazide 160/12.5MG Tablets, USP 90 Count1191160MSep-2018
      0591-2316-19Valsartan and Hydrochlorothiazide 160/12.5MG Tablets, USP 90 Count1191161MSep-2018
      0591-2316-19Valsartan and Hydrochlorothiazide 160/12.5MG Tablets, USP 90 Count1191162ASep-2018
      0591-2316-19Valsartan and Hydrochlorothiazide 160/12.5MG Tablets, USP 90 Count1219363MFeb-2019
      0591-2316-19Valsartan and Hydrochlorothiazide 160/12.5MG Tablets, USP 90 Count1219364MFeb-2019
      0591-2316-19Valsartan and Hydrochlorothiazide 160/12.5MG Tablets, USP 90 Count1219365AFeb-2019
      0591-2316-19Valsartan and Hydrochlorothiazide 160/12.5MG Tablets, USP 90 Count1225613AFeb-2019
      0591-2316-19Valsartan and Hydrochlorothiazide 160/12.5MG Tablets, USP 90 Count1233944MApr-2019
      0591-2316-19Valsartan and Hydrochlorothiazide 160/12.5MG Tablets, USP 90 Count1233945MApr-2019
      0591-2316-19Valsartan and Hydrochlorothiazide 160/12.5MG Tablets, USP 90 Count1253253MJul-2019
      0591-2316-19Valsartan and Hydrochlorothiazide 160/12.5MG Tablets, USP 90 Count1253254MJul-2019
      0591-2317-19Valsartan and Hydrochlorothiazide 160/25MG Tablets, USP 90 Count1191164MSep-2018
      0591-2317-19Valsartan and Hydrochlorothiazide 160/25MG Tablets, USP 90 Count1191165MSep-2018
      0591-2317-19Valsartan and Hydrochlorothiazide 160/25MG Tablets, USP 90 Count1191166MSep-2018
      0591-2317-19Valsartan and Hydrochlorothiazide 160/25MG Tablets, USP 90 Count1191167AOct-2018
      0591-2317-19Valsartan and Hydrochlorothiazide 160/25MG Tablets, USP 90 Count1225612MFeb-2019
      0591-2317-19Valsartan and Hydrochlorothiazide 160/25MG Tablets, USP 90 Count1250717MJul-2019
      0591-2317-19Valsartan and Hydrochlorothiazide 160/25MG Tablets, USP 90 Count1256111MJul-2019
      0591-2317-19Valsartan and Hydrochlorothiazide 160/25MG Tablets, USP 90 Count1288798MOct-2019
      0591-2318-19Valsartan and Hydrochlorothiazide 320/12.5MG Tablets, USP 90 Count1191185MSep-2018
      0591-2318-19Valsartan and Hydrochlorothiazide 320/12.5MG Tablets, USP 90 Count1191186MSep-2018
      0591-2318-19Valsartan and Hydrochlorothiazide 320/12.5MG Tablets, USP 90 Count1225615MFeb-2019
      0591-2318-19Valsartan and Hydrochlorothiazide 320/12.5MG Tablets, USP 90 Count1233948MFeb-2019
      0591-2318-19Valsartan and Hydrochlorothiazide 320/12.5MG Tablets, USP 90 Count1250718MAug-2019
      0591-2318-19Valsartan and Hydrochlorothiazide 320/12.5MG Tablets, USP 90 Count1253257MJul-2019
      0591-2319-19Valsartan and Hydrochlorothiazide 320/25MG Tablets, USP 90 Count1191188MSep-2018
      0591-2319-19Valsartan and Hydrochlorothiazide 320/25MG Tablets, USP 90 Count1191189MSep-2018
      0591-2319-19Valsartan and Hydrochlorothiazide 320/25MG Tablets, USP 90 Count1191190MSep-2018
      0591-2319-19Valsartan and Hydrochlorothiazide 320/25MG Tablets, USP 90 Count1199220MAug-2018
      0591-2319-19Valsartan and Hydrochlorothiazide 320/25MG Tablets, USP 90 Count1217576MJan-2019
      0591-2319-19Valsartan and Hydrochlorothiazide 320/25MG Tablets, USP 90 Count1217577MJan-2019
      0591-2319-19Valsartan and Hydrochlorothiazide 320/25MG Tablets, USP 90 Count1217578MJan-2019
      0591-2319-19Valsartan and Hydrochlorothiazide 320/25MG Tablets, USP 90 Count1220832MJan-2019
      0591-2319-19Valsartan and Hydrochlorothiazide 320/25MG Tablets, USP 90 Count1220833MFeb-2019
      0591-2319-19Valsartan and Hydrochlorothiazide 320/25MG Tablets, USP 90 Count1247283MJun-2019
      0591-2319-19Valsartan and Hydrochlorothiazide 320/25MG Tablets, USP 90 Count1247284MJun-2019
      0591-2319-19Valsartan and Hydrochlorothiazide 320/25MG Tablets, USP 90 Count1247285MJun-2019
      0591-2319-19Valsartan and Hydrochlorothiazide 320/25MG Tablets, USP 90 Count1247286MJun-2019
      0591-2319-19Valsartan and Hydrochlorothiazide 320/25MG Tablets, USP 90 Count1247287AJun-2019
      0591-2319-19Valsartan and Hydrochlorothiazide 320/25MG Tablets, USP 90 Count1280632MOct-2019
      0591-2319-19Valsartan and Hydrochlorothiazide 320/25MG Tablets, USP 90 Count1280633MOct-2019

      What to do

      Consumers with questions about the recall may contact Teva at (888) 838-2872, option 3, Monday – Friday, 9:00AM – 5:00PM (ET) or by email at druginfo@tevapharm.com.

      Teva Pharmaceuticals USA is recalling 29 lots of single and 51 lots of combination valsartan medicines distributed under the Actavis label, which are used...
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      Utz recalls Carolina Style Barbeque Potato Chips

      The product may contain soy, an allergen not declared on the label

      Utz Quality Foods is recalling its brand of Carolina Style Barbeque Potato Chips.

      The product may contain soy, an allergen not declared on the label.

      No illnesses associated with this recall have been reported to date.

      The following Carolina Style Barbeque Potato Chips are being recalled:

      Item DescriptionUPCExpiration Date FromExpiration Date To
      Utz 2.875 oz.0-41780-00153-5October 6thOctober 20th
      Utz 7.5 oz.0-41780-00049-1August 18thOctober 27th

      The recalled products were shipped to retail outlets in Alabama, Arkansas, Colorado, Connecticut, the District of Columbia, Delaware, Florida, Georgia, Illinois, Indiana, Kentucky, Louisiana, Massachusetts, Maryland, Maine, Mississippi, North Carolina, Nebraska, New Hampshire, New Jersey, New York, Ohio, Pennsylvania, Rhode Island, South Carolina, Tennessee, Texas, Utah, Virginia, Vermont and West Virginia.

      What to do

      Customers who purchased the recalled product and have an allergy or sensitivity to soy should not eat the product, but return it to the store where it was purchased for a full refund or exchange, or simply discard it.

      Consumers with questions may contact the firm at (800) 367-7629 Monday through Friday, 8:30 am – 5:00 pm (ET), or by email at customerservice@utzsnacks.com.

      Utz Quality Foods is recalling its brand of Carolina Style Barbeque Potato Chips.The product may contain soy, an allergen not declared on the label....
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      Water Pik recalls Sonic-Fusion flossing toothbrush

      The charging base may overheat

      Water Pik is recalling 3,800 Sonic-Fusion flossing toothbrushes.

      The charging base may overheat with localized melting and sparking, possibly causing fire, shock or burns.

      The company has received consumer reports of product malfunctioning in the U.S.

      The following models have been recalled:

      Name of ProductModelSerial/Lot Numbers
      Sonic-Fusion®SF-01

      SF01 17 06 01

      through

      SF01 18 06 28

      Sonic-Fusion®SF-02

      SF02 17 06 01

      through

      SF02 18 06 28

      The recalled product distributed between June 2017, and June 2018, throughout the U.S., and in Canada, and limited to professional educators, key opinion leaders, trade show customers and limited direct online sales.

      What to do

      Customers who have the recalled product should stop using it, immediately, unplug it, and return it to Water Pik.

      Consumers with questions or who want to receive a product return kit may contact the company at (800) 674-7718 from 7:00 a.m. – 5:00 p.m. (MDT) Monday through Friday, or by email at SonicFusion-Return@Waterpik.com.

      Water Pik is recalling 3,800 Sonic-Fusion flossing toothbrushes.The charging base may overheat with localized melting and sparking, possibly causing fi...
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      Papa John’s Salads and Produce recalls Superfood Salad

      The product contain peanuts, an allergen not declared on the label

      Papa John’s Salads and Produce of Tolleson, Ariz., is recalling 148 units of Superfood Salad.

      The products contain peanuts, an allergen not declared on the label.

      There have been no reported adverse reactions to this product to date.

      The following product, sold from the deli service case in stores in Arizona, California, Colorado, Montana, Nevada, Utah and Wyoming July 9 – 11, 2018, is being recalled:

      Product DescriptionConsumer
      UCP
      FacilityCityState
      Superfood Salad2541465####Fry's FoodScottsdaleAZ
      Superfood Salad2541465####Fry's FoodPhoenixAZ
      Superfood Salad2541465####Fry's FoodPhoenixAZ
      Superfood Salad2541465####Fry's FoodPeoriaAZ
      Superfood Salad2541465####Fry's FoodMesaAZ
      Superfood Salad2541465####Fry's FoodPrescottAZ
      Superfood Salad2541465####Fry's FoodSun City WestAZ
      Superfood Salad2541465####Fry's FoodOro ValleyAZ
      Superfood Salad2541465####Fry's FoodTucsonAZ
      Superfood Salad2070780####RalphsOrangeCA
      Superfood Salad2070780####RalphsSan DiegoCA
      Superfood Salad2070780####RalphsLos AngelesCA
      Superfood Salad2070780####RalphsPalm DesertCA
      Superfood Salad2070780####RalphsTemple CityCA
      Superfood Salad2070780####RalphsLa Canada FlintridgeCA
      Superfood Salad2070780####RalphsLong BeachCA
      Superfood Salad2070780####RalphsGlendaleCA
      Superfood Salad2070780####RalphsFullertonCA
      Superfood Salad2070780####RalphsWoodland HillsCA
      Superfood Salad2070780####RalphsCulver CityCA
      Superfood Salad2070780####RalphsSan PedroCA
      Superfood Salad2070780####RalphsEscondidoCA
      Superfood Salad2070780####RalphsPasadenaCA
      Superfood Salad2070780####RalphsFontanaCA
      Superfood Salad2070780####RalphsNorthridgeCA
      Superfood Salad2070780####RalphsHuntington BeachCA
      Superfood Salad2070780####RalphsIrvineCA
      Superfood Salad2070780####RalphsDowneyCA
      Superfood Salad2070780####RalphsBreaCA
      Superfood Salad2070780####RalphsLaguna HillsCA
      Superfood Salad2070780####RalphsMarina Del ReyCA
      Superfood Salad2070780####RalphsVeniceCA
      Superfood Salad2070780####RalphsLake ForestCA
      Superfood Salad2070780####RalphsBurbankCA
      Superfood Salad2070780####RalphsVenturaCA
      Superfood Salad2070780####RalphsIndioCA
      Superfood Salad2070780####RalphsStudio CityCA
      Superfood Salad2070780####RalphsChatsworthCA
      Superfood Salad2070780####RalphsNewbury ParkCA
      Superfood Salad2070780####RalphsSan BernardinoCA
      Superfood Salad2541465####King SoopersDenverCO
      Superfood Salad2541465####King SoopersColorado SpringsCO
      Superfood Salad2541465####King SoopersHighlands RanchCO
      Superfood Salad2541465####King SoopersAuroraCO
      Superfood Salad2541465####King SoopersBoulderCO
      Superfood Salad2541465####King SoopersGreeleyCO
      Superfood Salad2541465####King SoopersLittletonCO
      Superfood Salad2541465####King SoopersLongmontCO
      Superfood Salad2541465####King SoopersLovelandCO
      Superfood Salad2541465####King SoopersBroomfieldCO
      Superfood Salad2541465####King SoopersLakewoodCO
      Superfood Salad2541465####King SoopersEnglewoodCO
      Superfood Salad2541465####King SoopersFort CollinsCO
      Superfood Salad2541465####King SoopersWindsorCO
      Superfood Salad2541465####King SoopersCastle RockCO
      Superfood Salad2541465####King SoopersLafayetteCO
      Superfood Salad2541465####King SoopersBrightonCO
      Superfood Salad2541465####King SoopersMontroseCO
      Superfood Salad2541465####King SoopersDeltaCO
      Superfood Salad2541465####King SoopersGlenwood SpringsCO
      Superfood Salad2541465####King SoopersCortezCO
      Superfood Salad2541465####King SoopersCraigCO
      Superfood Salad2541465####King SoopersCanon CityCO
      Superfood Salad2541465####King SoopersDurangoCO
      Superfood Salad2541465####King SoopersAvonCO
      Superfood Salad2541465####King SoopersHotchkissCO
      Superfood Salad2541465####King SoopersEagleCO
      Superfood Salad2541465####King SoopersBuena VistaCO
      Superfood Salad2541465####King SoopersMontroseCO
      Superfood Salad2541465####King SoopersVailCO
      Superfood Salad2541465####King SoopersGrand JunctionCO
      Superfood Salad2541465####Smith's Food and DrugBozemanMT
      Superfood Salad2541465####Smith's Food and DrugKalispellMT
      Superfood Salad2541465####Smith's Food and DrugFarmingtonNM
      Superfood Salad2541465####Smith's Food and DrugLas VegasNV
      Superfood Salad2541465####Smith's Food and DrugHendersonNV
      Superfood Salad2541465####Smith's Food and DrugRenoNV
      Superfood Salad2541465####Smith's Food and DrugSalt Lake CityUT
      Superfood Salad2541465####Smith's Food and DrugLaytonUT
      Superfood Salad2541465####Smith's Food and DrugBrigham CityUT
      Superfood Salad2541465####Smith's Food and DrugClearfieldUT
      Superfood Salad2541465####Smith's Food and DrugOgdenUT
      Superfood Salad2541465####Smith's Food and DrugBountifulUT
      Superfood Salad2541465####Smith's Food and DrugSandyUT
      Superfood Salad2541465####Smith's Food and DrugWest JordanUT
      Superfood Salad2541465####Smith's Food and DrugVernalUT
      Superfood Salad2541465####Smith's Food and DrugMidvaleUT
      Superfood Salad2541465####King SoopersCheyenneWY
      Superfood Salad2541465####Smith's Food and DrugRock SpringsWY
      Superfood Salad2541465####Smith's Food and DrugCasperWY

      The recalled affected product has a Consumer UPC of 2541465#### or 2070780#### in which the last 4 digits (####) were the price of the product.

      What to do

      Customers who purchased the recalled product should discard it or return it to the place of purchase for a full refund.

      Consumers with questions may contact Papa John’s Salads and Produce at (480) 653-8901 Monday through Friday from 8am – 4pm (PST).

      Papa John’s Salads and Produce of Tolleson, Ariz., is recalling 148 units of Superfood Salad.The products contain peanuts, an allergen not declared on...
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      REV Recreation Group recalls Fleetwood Flair and Holiday Rambler Class A motorhomes

      The vehicles could experience an electrical short, increasing the risk of a fire

      REV Recreation Group (REV) is recalling five model year 2019 Fleetwood Flair and Holiday Rambler Class A motorhomes.

      These vehicles were manufactured with a non-flexible Romex wire inside the stationary bed frame, instead of with a flexible sheathed SJO cable. As a result, the Romex wire may become damaged from the movement of the slide-out.

      The damaged wiring could cause an electrical short, increasing the risk of a fire.

      What to do

      REV has repaired all of the affected Class A motorhomes while they were in dealer inventory by routing the wire harness through the plywood bed top and making sure that the flexible-sheathed SJO cable is routed through the bed and slide-out area, free of charge.

      All vehicles were repaired as of July 3, 2018.

      Owners may contact REV customer service at 1-800-509-3417. REV's number for this recall is 180618REV.

      REV Recreation Group (REV) is recalling five model year 2019 Fleetwood Flair and Holiday Rambler Class A motorhomes.These vehicles were manufactured wi...
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      Burton recalls snowboard boots

      The boots can release from the binding unexpectedly

      The Burton Corporation of Burlington, Vt., is recalling about 4,800 pair of snowboard boots.

      The boots can release from the binding unexpectedly, posing a fall hazard to the user.

      The company has received seven reports of the boots releasing from the binding unexpectedly. No injuries have been reported.

      This recall involves Step On snowboard boots from the winter 2017-2019 seasons. The recalled boots were sold in a variety of colors. The model name is printed on the inside of the boot tongue.

      Season

      Model Name

      Color

      Winter 17-18 Sales Sample

      PHOTON STEP-ON BOOT

      BLACK

      Winter 17-18 Sales Sample

      PHOTON STEP-ON BOOT

      BLUE PRINT

      Winter 17-18 Sales Sample

      FELIX STEP-ON BOOT

      BLACK

      Winter 17-18 Sales Sample

      FELIX STEP-ON BOOT

      STATIC

      Winter 17-18 Sales Sample

      RULER STEP-ON BOOT

      BLACK

      Winter 17-18 Sales Sample

      RULER STEP-ON BOOT

      GREY TIE DYE

      Winter 17-18 Sales Sample

      RULER STEP-ON BOOT

      TAN

      Winter 17-18 Sales Sample

      LIMELIGHT STEP-ON BOOT

      BLACK

      Winter 17-18 Sales Sample

      LIMELIGHT STEP-ON BOOT

      BLACK/MULTI

      Winter 17-18 Sales Sample

      LIMELIGHT STEP-ON BOOT

      TAN

      Winter 17-18 Production

      PHOTON STEP ON BOOT

      BLACK

      Winter 17-18 Production

      PHOTON STEP ON BOOT

      BLUE PRINT

      Winter 17-18 Production

      FELIX STEP ON BOOT

      BLACK

      Winter 17-18 Production

      FELIX STEP ON BOOT

      STATIC

      Winter 17-18 Production

      RULER STEP ON BOOT

      BLACK

      Winter 17-18 Production

      RULER STEP ON BOOT

      GREY TIE DYE

      Winter 17-18 Production

      LIMELIGHT STEP ON BOOT

      BLACK

      Winter 17-18 Production

      LIMELIGHT STEP ON BOOT

      BLACK/MULTI

      Winter 18-19 Sales Sample

      PHOTON STEP ON BOOT

      CLOVER

      Winter 18-19 Sales Sample

      PHOTON STEP ON BOOT

      BLACK

      Winter 18-19 Sales Sample

      FELIX STEP ON BOOT

      BLACK

      Winter 18-19 Sales Sample

      RULER STEP ON BOOT

      BLACK

      Winter 18-19 Sales Sample

      RULER STEP ON BOOT

      BLACK/CAMO

      Winter 18-19 Sales Sample

      LIMELIGHT STEP ON BOOT

      BLACK

      Winter 18-19 Sales Sample

      LIMELIGHT STEP ON BOOT

      MIDNITE BLOOM

      Winter 18-19 Sales Sample

      ION STEP ON BOOT

      BLACK

      Winter 18-19 Sales Sample

      ZIPLINE STEP ON BOOT

      BLACK

      Winter 18-19 Sales Sample

      PHOTON STEP ON – ASIAN FIT BOOT

      CLOVER

      Winter 18-19 Sales Sample

      PHOTON STEP ON – ASIAN FIT BOOT

      BLACK

      The boots, manufactured in China, were sold at Burton and other specialty stores nationwide and online at Burton.com and other websites from November 2016, through December 2017, for between $300 and $400.

      What to do

      Consumers should immediately stop using the recalled snowboard boots and contact Burton to receive a free new heel cleat. Burton is contacting all known purchasers directly.

      Consumers may contact Burton at (800) 881-3138 from 8 a.m. to 6 p.m. (ET) Monday through Friday, by email at info@burton.com or online at www.burton.com and click on “Step On Heel Cleat Update” for more information.

      The Burton Corporation of Burlington, Vt., is recalling about 4,800 pair of snowboard boots.The boots can release from the binding unexpectedly, posing...
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      Porsche recalls various Panamera model vehicles

      The connecting links may detach from the rear-axle anti-roll bar

      Porsche Cars North America is recalling 715 model year 2017-2018 Panamera 4S, Panamera Turbo and Panamera Turbo Executive vehicles, and model year 2018 Panamera Turbo S E-Hybrid, Panamera Turbo S E-Hybrid Executive, Panamera 4S Sport Turismo, Panamera Turbo Sport Turismo, Panamera Turbo S E-Hybrid Sport Turismo and Panamera 4S Executive vehicles.

      The connecting links may detach from the rear-axle anti-roll bar potentially damaging the surrounding suspension parts and affecting the vehicle's handling, increasing the risk of a crash.

      What to do

      Porsche will notify owners, and dealers will replace the connecting links for the anti-roll bar, free of charge.

      The manufacturer has not yet provided a notification schedule.

      Owners may contact Porsche customer service at 1-800-767-7243. Porsche's number for this recall is AJ06.

      Porsche Cars North America is recalling 715 model year 2017-2018 Panamera 4S, Panamera Turbo and Panamera Turbo Executive vehicles, and model year 2018 Pan...
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      Ortovox recalls avalanche transceivers

      The transceiver can fail to work properly due to a software error

      Ortovox of Germany is recalling about 27,000 avalanche transceivers sold in the U.S. and Canada.

      The transceiver can fail to work properly due to a software error and fail to transmit the position of survivors of an avalanche, resulting in delayed search and rescue operations.

      No incidents or injuries have been reported.

      This recall involves Ortovox avalanche transceivers, model numbers 1137000006, 1137000001 and 1137000002.

      They were sold in black/blue (model number 1137000006), black/black (model number 1137000001) and neon green (model number 1137000002).

      The transceiver is used as a beacon to locate an individual in the event of avalanche burial.

      ORTOVOX and 3+ are printed on the top of the device. In the open/receive position, the top half of the transceiver displays a blue screen with green border that displays an image and distance reading of the buried individual.

      The transceivers measure about 5 inches long by 3 inches wide by 1 inch thick in the closed/transmit position. All transceivers manufactured from 2010 through 2018 are included in the recall.

      The manufacture date is printed inside the battery door on the back of the transceiver with a roman numeral representing the quarter of the year and a two digit number referring to the year.

      For example, a manufacture date of IV/17 represents the fourth quarter. The year of manufacture is five years earlier. In this case, the transceiver was manufactured in the fourth quarter of 2012.

      The transceivers, manufactured in Germany, were sold at outdoor specialty stores, ski shops nationwide and direct to avalanche professionals, search and rescue personnel and mountain guides from July 2010. through April 2018. for about $350.

      What to do

      Consumers should immediately stop using the recalled transceivers and return them to Ortovox for a free repair, including free shipping.

      Consumers may contact Ortovox toll-free at 877-384-9252 from 8 a.m. to 5 p.m. (MT) Monday through Thursday, by email at ortovox.warranty@deuterusa.com or online at www.ortovox.com and click on RECALL 3+ for more information.

      Ortovox of Germany is recalling about 27,000 avalanche transceivers sold in the U.S. and Canada.The transceiver can fail to work properly due to a soft...
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      Grand Design recalls Solitude fifth-wheel trailers

      The liquid propane gas line may contact the underside of the hot grill

      Grand Design RV is recalling 200 model year 2018-2019 Grand Design Solitude fifth-wheel trailers.

      The liquid propane (LP) gas line on the optional pull-out outside kitchen may contact the underside of the hot grill.

      Contact with the hot grill may result in a propane leak, increasing the risk of a fire.

      What to do

      Grand Design will notify owners, and dealers will re-route the LP gas line to prevent it from contacting the bottom of the grill, free of charge.

      The recall is expected to begin July 16, 2018.

      Owners may contact Grand Design RV customer service at 1-574-825-9679. Grand Design's number for this recall is 900013.

      Grand Design RV is recalling 200 model year 2018-2019 Grand Design Solitude fifth-wheel trailers.The liquid propane (LP) gas line on the optional pull-...
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      Saje recalls Splish Splash Gentle Baby Wash

      The product may contain Pseudomonas aeruginosa bacteria

      Saje Natural Wellness is recalling Splish Splash Gentle Baby Wash found in the Wee and Well Gentle Baby Care Kit.

      The product may contain Pseudomonas aeruginosa bacteria, an opportunistic pathogen that causes infection and results in bacteria in the blood, particularly in individuals with compromised immune systems.

      There are no reported adverse reactions in the U.S. to date.

      The following product, sold in the U.S. through Saje retail locations in California, New Jersey and New York, and online in the U.S. and internationally, is being recalled:

      Brand Name & Product NameProduct SKUPackage SizeLot NumberExpiry Date
      Saje Natural Wellness Splish Splash Gentle Baby Wash700552 
      (USA/Int’l)
      8.5 fl. oz.814020All expiry dates
      Saje Natural Wellness Splish Splash Gentle Baby Wash (found in Wee and Well Gentle Baby Care Kit)700561 
      (USA/Int’l)
      1.7 fl. oz.814020All expiry dates

      The 6-digit lot number is located on the information panel on the back of the product, below the SKU number.

      What to do

      Customers who purchased the recalled product should stop using it and return it to a Saje retail outlet, for a full refund.

      Consumers with questions may contact the company at (877) 275-7253 from 5:00AM – 8:00PM (PST) Monday through Friday, and 8:00AM – 5:00PM (PST) Saturday and Sunday, or by email at hello@saje.com to receive a full refund.

      Saje Natural Wellness is recalling Splish Splash Gentle Baby Wash found in the Wee and Well Gentle Baby Care Kit.The product may contain Pseudomonas ae...
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      Lamborghini recalls Aventador Coupes and Roadsters

      The engine may stall unexpectedly, posing a crash risk

      Automobili Lamborghini is recalling 1,700 model year 2012-2018 Lamborghini Aventador Coupes and Roadsters.

      The engine may stall unexpectedly during certain driving conditions such as when the accelerator pedal is released below 2000 rpms while the transmission is automatically down-shifting to a lower gear.

      An engine stall can increase the risk of a crash.

      What to do

      Lamborghini will notify owners, and dealers will install updated engine software, free of charge.

      The recall is expected to begin August 3, 2018.

      Owners may contact Lamborghini customer service at 1-866-681-6276. Lamborghini's number for this recall is L73X-R.02.18.

      Automobili Lamborghini is recalling 1,700 model year 2012-2018 Lamborghini Aventador Coupes and Roadsters.The engine may stall unexpectedly during cert...
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      AJ International Trading recalls Wulama brand Fish Tofu

      The product may contain egg, and sesame allergens not declared on the label

      AJ International Trading is recalling Wulama brand Fish Tofu.

      The product may contain egg, and sesame allergens not declared on the label.

      No reactions associated with the consumption of this product have been reported.

      The following product, sold in Ontario, Canada, is being recalled:

      Brand NameCommon NameSizeCode(s) on ProductUPC
      Wulama (Chinese characters only)Fish Tofu95 gAll codes where egg and sesame are not declared on the label6 936158 282279

      What to do

      Customers who purchased the recalled product and have an allergy to egg or sesame, should not consume it, but discard it or return it to the place of purchase.

      AJ International Trading is recalling Wulama brand Fish Tofu.The product may contain egg, and sesame allergens not declared on the label.No reactio...
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      Newmar recalls Mountain Aire, London Aire, Essex and King Aire motorhomes

      The vehicles' windshield wiper arms may not contact the windshield properly

      Newmar Corporation is recalling 77 model year 2018-2019 Newmar Mountain Aire, London Aire, Essex and King Aire motorhomes.

      The vehicles are equipped with windshield wipers that may have an incorrect bend, possibly preventing the wiper arms from properly contacting the windshield.

      If the wipers do not properly contact the windshield, the driver's visibility may be reduced, increasing the risk of a crash.

      What to do

      Newmar will notify owners, and dealers will replace the wiper arms, free of charge.

      The recall is expected to begin August 8, 2018.

      Owners may contact Newmar customer service at 1-800-731-8300.

      Newmar Corporation is recalling 77 model year 2018-2019 Newmar Mountain Aire, London Aire, Essex and King Aire motorhomes. The vehicles are equipped wit...
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      Sandoz and Novartis recall prescription drug blister packages

      The packaging is not child resistant as required by law

      Sandoz Inc., of Princeton, N.J., and Novartis Pharmaceuticals Corp., of East Hanover, N.J., are recalling about 470, 000 blister packages of prescription medication.

      The prescription drug packaging is not child resistant as required by the Poison Prevention Packaging Act, posing a poisoning risk if swallowed by children.

      The firms have received one report of a child ingesting haloperidol from a blister pack.

      This recall involves blister packages of prescription drugs from Novartis and Sandoz. The drugs are packaged with 3 to 10 tablets per blister card.

      The recalled Novartis prescription blister packages have “Novartis,” the name of the drug, dosage, NDC, lot number and expiration date printed on the cartons and the blister cards. The recall includes the following:

      Recalled Novartis Prescription Drugs

      NDC Numbers

      Tablet Strength

      Carton Configuration

      Lot Numbers

      Expiration Date

      Zofran ODT®

      0078-0679-61

      0078-0679-19

      4 mg

      30 count: 3 cards with 10 tablets each

      1657088

      Dec 2019

      Zofran ODT®

      0078-0680-61

      0078-0680-19

      8 mg

      30 count: 3 cards with 10 tablets each

      1641546

      Oct 2019

      Entresto® (sacubitril/valsartan)

      0078-0659-61

      0078-0659-35

      24 mg/ 26 mg

      100 count: 10 cards with 10 tablets each

      FX000005

      FX000004

      FX000003

      F0010

      F0009

      F0007

      Apr 2020

      Apr 2020

      Sep 2019

      Nov 2018

      Aug 2018

      Jul 2018

      Entresto® (sacubitril/valsartan)

      0078-0777-61

      0078-0777-35

      49 mg/ 51 mg

      100 count: 10 cards with 10 tablets each

      FX000001

      F0006

      F0005

      F0004

      Dec 2019

      Oct 2019

      Aug 2019

      Oct 2018

      Entresto® (sacubitril/valsartan)

      0078-0696-61

      0078-0696-35

      97 mg/ 103 mg

      100 count: 10 cards with 10 tablets each

      FX000002

      F0007

      F0006

      F0005

      F0004

      Mar 2020

      Feb 2020

      Dec 2019

      Dec 2018

      Oct 2018

      The recalled Sandoz prescription blister packages have “Sandoz,” the name of the drug, dosage, NDC and lot number printed on the cartons and the blister cards.

      Lot numbers are listed at www.us.sandoz.com/patients-customers/product-safety-notices.

      The recall includes the following:

      Recalled Sandoz Prescription Drugs

      Tablet Strength

      NDC Numbers

      Carton Configuration

      Azithromycin Tablets

      250 mg

      0781-5776-06

      0781-5776-69

      50 count: 5 cards with 10 tablets each

      Donepezil ODT  Tablets

      5 mg

      0781-5276-06

      0781-5276-64

      30 count: 3 cards with 10 tablets each

      Donepezil ODT Tablets

      10 mg

      0781-5277-06

      0781-5277-64

      30 count: 3 cards with 10 tablets each

      Haloperidol Tablets

      0.5 mg

      0781-1391-13

      100 count: 10 cards with 10 tablets each

      Haloperidol Tablets

      1 mg

      0781-1392-13

      100 count: 10 cards with 10 tablets each

      Haloperidol Tablets

      2 mg

      0781-1393-13

      100 count: 10 cards with 10 tablets each

      Haloperidol Tablets

      5 mg

      0781-1396-13

      100 count: 10 cards with 10 tablets each

      Haloperidol Tablets

      10 mg

      0781-1397-13

      100 count: 10 cards with 10 tablets each

      Imipramine HCl Tablets

      25 mg

      0781-1764-13

      100 count: 10 cards with 10 tablets each

      Imipramine HCl Tablets

      50 mg

      0781-1766-13

      100 count: 10 cards with 10 tablets each

      Isosorbide Dinitrate (ISDN) Tablets

      10 mg

      0781-1556-13

      100 count: 10 cards with 10 tablets each

      Isosorbide Dinitrate (ISDN) Tablets

      20 mg

      0781-1695-13

      100 count: 10 cards with 10 tablets each

      Naratriptan Tablets

      2.5 mg

      0781-5527-06

      0781-5527-37

      9 count: 1 card with 9 tablets

      Ondansetron Tablets

      8 mg

      0781-1681-33

      3 count: 1 card with 3 tablets

      Ondansetron ODT

      4 mg

      0781-5238-06

      0781-5238-64

      30 count: 3 cards with 10 tablets each

      Ondansetron ODT

      8 mg

      0781-5239-06

      0781-5239-64

      30 count: 3 cards with 10 tablets each

      Ondansetron ODT

      8 mg

      0781-5239-06

      0781-5239-80

      10 count: 1 card with 10 tablets

      Perphenazine Tablets

      2 mg

      0781-1046-13

      100 count: 10 cards with 10 tablets each

      Perphenazine Tablets

      4 mg

      0781-1047-13

      100 count: 10 cards with 10 tablets each

      Perphenazine Tablets

      8 mg

      0781-1048-13

      100 count: 10 cards with 10 tablets each

      Risperidone ODT

      0.5 mg

      0781-5310-06

      0781-5310-08

      28 count: 7 cards with 4 tablets each

      Risperidone ODT

      1 mg

      0781-5311-06

      0781-5311-08

      28 count: 7 cards with 4 tablets each

      Risperidone ODT

      2 mg

      0781-5312-06

      0781-5312-08

      28 count: 7 cards with 4 tablets each

      Risperidone ODT

      3 mg

      0781-5313-06

      0781-5313-08

      28 count: 7 cards with 4 tablets each

      Risperidone ODT

      4 mg

      0781-5314-06

      0781-5314-08

      28 count: 7 cards with 4 tablets each

      The recalled products, manufactured in Croatia, India, Ireland, Israel, Italy, Singapore, Spain, UK and U.S., were sold at clinics and pharmacies nationwide as a prescribed medicine from September 2016, to June 2018, at prices varying based on quantities prescribed, health insurance terms and other factors.

      What to do

      Consumers should immediately secure the blister cards to keep them out of the sight and reach of children and contact Novartis or Sandoz for further instructions. Novartis and Sandoz advise that consumers should continue to use the medication as directed once the blister packages are secured.

      Consumers may contact Sandoz and Novartis toll-free at 888-669-6682 from Monday to Friday, 8 a.m. to 8 p.m. (ET) and Saturday and Sunday, 9 a.m. to 6 p.m. (ET) or online at www.us.sandoz.com and click on “Patients and Customers” then “Product Safety Notices,” or at www.pharma.us.novartis.com and click on banner “Novartis recalls select product blister packs.”

      Sandoz Inc., of Princeton, N.J., and Novartis Pharmaceuticals Corp., of East Hanover, N.J., are recalling about 470, 000 blister packages of prescription m...
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      Forest River Salem and Wildwood recreational trailers recalled

      The trailers could suffer axle failure

      Forest River is recalling 152 Forest River Salem and Wildwood recreational trailers.

      The vehicles have an axle equalizer that can allow the axle to contact the chassis, which could result in axle failure and increase the risk of a crash.

      What to do

      Forest River has notified owners, and dealers will replace the axle equalizer kit with a taller equalizer kit, free of charge.

      The recall began on June 27, 2018.

      Owners may contact Forest River customer service at 1-574-534-4058. Forest River's number for this recall is 72-0753.

      Forest River is recalling 152 Forest River Salem and Wildwood recreational trailers.The vehicles have an axle equalizer that can allow the axle to cont...
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      Thor recalls motorhomes built on modified Ford E-450 chassis

      The axle may separate and cause a loss of control

      Thor Motor Coach (TMC) is recalling 691 model year 2019 Thor Four Winds, Chateau, Freedom Elite, Majestic, Outlaw, Quantum and Vegas motorhomes built on modified Ford E-450 chassis.

      The U-bolts on the rear axle that hold the leaf spring and rear axle together may have been insufficiently tightened.

      The loose U-bolts may further loosen or break allowing the axle to separate and cause a loss of control, increasing the risk of a crash.

      What to do

      TMC has notified owners, and dealers will tighten U-bolts to the proper torque, free of charge.

      The recall began on June 22, 2018.

      Owners may contact TMC customer service at 1-877-855-2867. TMC's number for this recall is RC000156.

      Thor Motor Coach (TMC) is recalling 691 model year 2019 Thor Four Winds, Chateau, Freedom Elite, Majestic, Outlaw, Quantum and Vegas motorhomes built on mo...
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      Keystone recalls Cougar recreational trailers

      The outdoor propane grill may not have enough clearance from the heated area.

      Keystone RV Company is recalling 5,107 model year 2018-2019 Keystone Cougar recreational trailers equipped with an outdoor propane grill.

      The outdoor propane grill is installed in a wooden assembly that may not have enough clearance from the heated area.

      If the wooden assembly is exposed to high temperatures, there would be an increased risk of a fire.

      What to do

      Keystone will notify owners, and dealers will replace the wooden assembly with a metal assembly, free of charge.

      The recall is expected to begin July 31, 2018.

      Owners may contact Keystone customer service at 1-866-425-4369. Keystone's number for this recall is 18-322.

      Keystone RV Company is recalling 5,107 model year 2018-2019 Keystone Cougar recreational trailers equipped with an outdoor propane grill.The outdoor pr...
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      LL’S Magnetic Clay expands recall of Prescript-Assist dietary supplement

      The product may contain undeclared allergens including almonds, crustaceans, dairy, casein, eggs and peanuts

      LL’s Magnetic Clay of Austin, Texas, is expanding its earlier recall to include all lots of Prescript-Assist, a dietary supplement it marketed until late 2017.

      The product may contain allergens including almonds, crustaceans, dairy, casein, eggs and peanuts, allergens not declared on the label.

      No illnesses regarding these products have been reported to date.

      The recalled product was sold nationwide online sales on the company's website and by brick and mortar retailers.

      It was also available through distributors other than LL’s Magnetic Clay that purchased the product from the same source.

      The recall includes all lots sold between 1/29/2015 – 12/31/2017 in white bottles contain capsules in quantities of either 60 or 90 capsules per bottle.

      What to do

      Customers who purchased the recalled product should discontinue using it and return it to LL’s Magnetic Clay for a full refund.

      Consumers with questions may contact the company at (800) 257-3315 Monday – Friday from 9am – 5pm.

      LL’s Magnetic Clay of Austin, Texas, is expanding its earlier recall to include all lots of Prescript-Assist, a dietary supplement it marketed until late 2...
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      Camso Recalls dirt to snow bike conversion kits

      The bolts on the brakes can loosen

      Camso Inc. of Quebec, Canada, is recalling about 910 Camso dirt to snow bike conversion kits.

      The bolts on the brakes can loosen, posing a crash or impact hazard.

      The company has received two reports involving the DTS 129 brake disc bolts loosening and seven reports involving the Yeti Snow MX brake disc bolts loosening. No injuries have been reported.

      This recall involves model year 2018 Camso DTS 129 and Yeti Snow MX kits that are used to convert off road motorcycles or dirt bikes to track and ski vehicles.

      The DTS 129 kits have a serial number starting with 9025ICEXXXX located on the conversion system frame.

      The Yeti Snow MX kits have a serial number starting with YE3XXXX located under the system.

      DTS 129 and the Camso logo or the Yeti logo are printed on the side of the product.

      The conversion kits, manufactured in Canada, were sold at Powersports dealers nationwide from August 2017, through May 2018, for about $4,800 for the DTS and $7,700 for the Yeti.

      What to do

      Consumers should immediately stop using bikes with the recalled conversion kits and contact an authorized Camso dealer for a free repair.

      Consumers may contact Camso toll-free at (866) 533-0008 from 8 a.m. to 5 p.m. (ET) Monday through Friday or online at www.camso.co and click on “service and support” for more information

      Camso Inc. of Quebec, Canada, is recalling about 910 Camso dirt to snow bike conversion kits.The bolts on the brakes can loosen, posing a crash or impa...
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      Mazda recalls model year 2005-2006 MPVs

      The passenger front airbag inflators may explode

      Mazda North America Operations is recalling 2,539 model year 2005-2006 MPVs sold, or ever registered, in Alaska, Colorado, Connecticut, Idaho, Iowa, Maine, Massachusetts, Michigan, Minnesota, Montana, New Hampshire, New York, North Dakota, Oregon, Rhode Island, South Dakota, Utah, Vermont, Washington, Wisconsin and Wyoming.

      These vehicles are equipped with air bag inflators assembled as part of the passenger frontal air bag modules used as original equipment or replacement equipment.

      In the event of a crash necessitating deployment of the passenger frontal air bag, these inflators may explode due to propellant degradation occurring after long-term exposure to absolute humidity and temperature cycling.

      An inflator explosion may result in metal fragments striking the vehicle occupants resulting in serious injury or death.

      What to do

      Mazda will notify owners, and dealers will replace the front passenger air bag inflator with an alternate inflator, free of charge.

      The recall is expected to begin July 2018.

      Owners may contact Mazda customer service at 1-800-222-5500, Option 4. Mazda's number for this recall is 2618F.

      Mazda North America Operations is recalling 2,539 model year 2005-2006 MPVs sold, or ever registered, in Alaska, Colorado, Connecticut, Idaho, Iowa, Maine,...
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      Model year 2015-2016 Mobility Ventures MV-1 vehicles recalled

      The turn signal malfunction warning may not work

      Mobility Ventures is recalling 977 model year 2015-2016 Mobility Ventures MV-1 vehicles.

      If a rear turn signal stops working properly, the vehicle will not adjust the turn signal flash rate frequency to warn the driver that a turn signal is not working correctly.

      If unaware that his turn signals are not working properly, the driver may continue to use the vehicle with turn signals that may not communicate the driver's intentions, increasing the risk of a crash.

      What to do

      The remedy for this recall is still under development.

      The recall is expected to begin July 30, 2018. Owners may contact Mobility Ventures customer service at 1-877-681-3678.

      Mobility Ventures is recalling 977 model year 2015-2016 Mobility Ventures MV-1 vehicles.If a rear turn signal stops working properly, the vehicle will...
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      Blissful Remedies recalls kratom powder capsules

      The products may be contaminated with Salmonella

      Blissful Remedies is recalling one lot of kratom ( mitragyn a speciosa) powder products.

      The product may be contaminated with Salmonella.

      There are no reports to date of adverse events related to this recall.

      The following products, manufactured, processed, packed and/or held, between March 1, 2018, and April 30, 2018, lot #12710 with expiration 03/2019 embedded on the top of package, are being recalled:

      Products LabelSizePackaging
      Red Maeng Da (100% Mitragyna 
      Speciosa)
      50 capsulesWhite Foil Pouches
      Gold Series Ultra Enhanced Indo 
      (100% Mitragyna Speciosa)
      50 capsulesWhite Foil Pouches
      Kratom+CBD., CBD infused
      Maeng Da
      50 capsulesWhite Foil Pouches

      The recalled products sold in retail stores in Alaska, Arizona, California, Florida, Georgia, Hawaii, Illinois, Kansas, Kentucky, Connecticut, Massachusetts, Michigan, Minnesota, Missouri, Mississippi, Nebraska, New Jersey, New Mexico, New York, Ohio, Oklahoma, Pennsylvania, Puerto Rico, South Dakota, Texas and Virginia.

      What to do

      Customers who purchased the recalled products should return them to the company cor credit or discard them.

      Consumers with questions may contact the company at (800) 435-8533, 9 am – 6 pm (CT), Monday through Friday or by email at fdarecall@blissfulremedies.com.

      Blissful Remedies is recalling one lot of kratom ( mitragyn a speciosa) powder products.The product may be contaminated with Salmonella.There are n...
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      Canadian Tire Corporation recalls MASTER Chef BBQ Igniter lighters

      The lighters do not meet the Lighters Regulations in Canada

      Canadian Tire Corporation Limited is recalling about 52,600 MASTER Chef BBQ Igniter lighters.

      The lighters do not meet the Lighters Regulations in Canada and may pose a fire or burn hazard. Specifically, they may exceed the allowable flame height during ignition, exhibit an abnormal, sudden increase in flame height, continue to burn after the trigger mechanism has been released.

      The company has received no reports of incidents or injuries.

      The following product, which has an adjustable flame height and is 285 mm long with a grey handle & black barrel, and was sold in Canada is being recalled:

      Impacted lighters can be

      identified with the following

      information on the rear packaging

      of the product:

      Product

      Number

      Lot #

      DoM

      UPC

      076-2044

      AD6523

      /G35J

      2016-02-01

      64599

      0215739

      What to do

      Consumers should immediately stop using the recalled lighters and return the product to their local Canadian Tire store for a refund.

      Canadian Tire Corporation Limited is recalling about 52,600 MASTER Chef BBQ Igniter lighters.The lighters do not meet the Lighters Regulations in Canad...
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      Various Nanfang, Want Want and Chencun brand products recalled

      The products may contain peanuts, walnuts and milk, allergens not declared on the label.

      AJ International Trading is recalling certain Nanfang brand, Want Want brand and Chencun brand products from the marketplace.

      The products may contain peanuts, walnuts and milk, allergens not declared on the label.

      There have been no reported reactions associated with the consumption of these products.

      The following products, sold in retail stores throughout Ontario, Canada, are being recalled:

      Brand NameCommon NameSizeUPC
      NanfangBlack Sesame Paste (Walnut)600 g6 901333 110739
      NanfangBlack Sesame Paste (Low sugar)600 g6 901333 980400
      Want WantShake Jelly (Strawberry)132 g6 920658 210436
      Want WantShake Jelly (Green Tea)132 g6 920658 267140
      Chencun (Chinese Characters only)Instant Noodles100 g × 46 942628 031070

      What to do

      Customers who purchased the recalled products and have an allergy to peanut, walnut or milk should not consume them, but dicard them or return them to the store where purchased.

      AJ International Trading is recalling certain Nanfang brand, Want Want brand and Chencun brand products from the marketplace.The products may contain p...
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      May Flower International recalls soda crackers

      The product may contain milk, an allergen not declared on the label

      May Flower International of Maspeth, N.Y., is recalling 4.4-oz., packages of “3+2 Soda Crackers.”

      The product may contain milk, an allergen not declared on the label.

      No illnesses or allergic reactions involving this product have been reported to date.

      The recalled product, which comes in a 4.4-oz., yellow plastic package and is un-coded., was sold in retail stores nationwide.

      What to do

      Customers who purchased the recalled product should return it to the place of purchase for a full refund.

      Consumers with questions may contact the company at (718) 366-8668.

      May Flower International of Maspeth, N.Y., is recalling 4.4-oz., packages of “3+2 Soda Crackers.”The product may contain milk, an allergen not declared...
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      Northwood Nash 24M and Nash 29S travel trailers recalled

      The tires may rub against the shocks

      Northwood Manufacturing is recalling nine model year 2019 Northwood Nash 24M and Nash 29S travel trailers.

      The tires may rub against the shocks and cause damage to the tires, resulting in tire failure and increasing the risk of a crash.

      What to do

      Northwood will notify owners, and dealers will re-mount the shocks to provide clearance between the shocks and tires, free of charge.

      The recall is expected to begin in July 2018.

      Owners may contact Northwood customer service at 1-800-766-6274. Northwood's number for this recall is 2018-001.

      Northwood Manufacturing is recalling nine model year 2019 Northwood Nash 24M and Nash 29S travel trailers.The tires may rub against the shocks and caus...
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      United States Bakery recalls Naked Bread hamburger buns

      The product may contain milk, an allergen not declared on the label

      United States Bakery of Portland, Ore., is recalling Naked Bread hamburger buns.

      The product may contain milk, an allergen not declared on the label.

      No illnesses have been reported to date.

      It is sold in the bread aisle at retail stores and was distributed directly in Northern California, Idaho, Montana, Oregon, Utah, Washington between June 2, 2018 and July 2, 2018.

      The recalled product is packaged in low density polyethylene bag and identified as “Naked Bread Hamburger Buns #NothingToHide, 8 pack, Net wt. 16.5 oz., UPC #72220 11075. The affected lot codes are F6 Best By June 16, 2018, through July 16, 2018.

      It was sold in the bread aisle at retail stores and distributed directly in Northern California, Idaho, Montana, Oregon, Utah and Washington from June 2, 2018 – July 2, 2018.

      What to do

      Customers who purchased the recalled product and have an allergy or severe sensitivity to milk may return product to a place of purchase for full refund.

      Consumers with questions may contact the company at (503) 232-2191 x4999 between 8 am – 5 pm (PST), Monday-Friday, or online at https://www.nakedbreads.com/.

      United States Bakery of Portland, Ore., is recalling Naked Bread hamburger buns.The product may contain milk, an allergen not declared on the label....
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      Whole Foods recalls Oatmeal Raisin Cookies

      The products contain soy flour, an allergen not listed on the label

      Whole Foods Market is recalling Whole Foods Market brand oatmeal raisin cookies from stores in eight states.

      The products contain soy flour, an allergen that's not listed on the label.

      No illnesses have been reported to date.

      The recalled cookies, packaged in an 18-count plastic container with a PLU beginning with 23209 and sell by dates from June 4 through July 8, 2018, were sold in Illinois, Indiana, Iowa, Michigan, Minnesota, Missouri, Nebraska and Wisconsin.

      What to do

      Customers who purchased the recalled products should bring a valid receipt into stores for a full refund.

      Consumers with questions may call (844) 936-8255 from 7:00 a.m. – 10:00 p.m. (CST) Monday through Friday, or 8:00 a.m. – 6:00 p.m. (CST) Saturday through Sunday.

      Whole Foods Market is recalling Whole Foods Market brand oatmeal raisin cookies from stores in eight states.The products contain soy flour, an allergen...
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      L&D Market recalls chicken wraps

      The products contain milk, an allergen not declared on the label

      L&D Market of Boston, Mass., is recalling approximately three pounds of chicken wraps.

      The products contain milk, an allergen not declared on the label.

      There have been no confirmed reports of adverse reactions due to consumption of these products.

      The following items, produced on June 21, June 26, and June 27, 2018, are being recalled:

      • 7.5-oz. plastic wrapped packages containing “Fresh. LOCAL. TASTY. EVERY DAY. WASABI CHICKEN WRAP,” with “SELL BY” dates of June 25, June 30 and July 1, 2018.
      • 7.5-oz. plastic wrapped packages containing “In-House Marketplace WASABI CHICKEN WRAP,” with a “SELL BY” date of June 25, 2018.

      The recalled products bearing establishment number “P-40171” inside the USDA mark of inspection, were shipped to retail locations in Cambridge, Massachusetts.

      What to do

      Customers who purchased the recalled should not consume them, but discard them or return them to the place of purchase.

      Consumers with questions about the recall may contact Freddy Noviello at (617) 567-9725.

      L&D; Market of Boston, Mass., is recalling approximately three pounds of chicken wraps.The products contain milk, an allergen not declared on the label...
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      Wish-Bone House Italian Salad Dressing recalled

      The product contains milk and egg, allergens not declared on the label

      Pinnacle Foods is recalling a limited quantity of Wish Bone House Italian Salad Dressing.

      The product contains milk and egg, allergens not declared on the label

      No illnesses have been reported to date.

      The following item, produced on March 19, 2018, is being recalled:

      FLAVORCASE LOT 
      CODE
      ITEM NUMBER #Best if Used By Date
      (found on neck label of bottle)
      Wish Bone House Italian 6/15 oz.4913019S51004132100648Jan 13 19

      A total of, 7,768 cases of the recalled product in 15-oz., bottles were sold nationwide with a “Best If Used By” date of Jan 13 19 on the neck label of the bottle.

      What to do

      Customers who purchased the recalled product should not consume it, but return it to the place of purchase for a full refund.

      Consumers with questions may contact Pinnacle Foods at (888) 299-7646 daily from 9 a.m. – 5 p.m. (ET).

      Pinnacle Foods is recalling a limited quantity of Wish Bone House Italian Salad Dressing.The product contains milk and egg, allergens not declared on t...
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      LL’s Magnetic Clay recalls Prescript-Assist dietary supplement

      The product may contain undeclared allergens including almonds, crustaceans, dairy, casein, eggs and peanuts

      LL’s Magnetic Clay of Austin, Texas, is recalling certain lots of Prescript-Assist, a dietary supplement it marketed until late 2017.

      The product may contain almonds, crustaceans, dairy, casein, eggs and peanuts -- allergens not declared on the label.

      No illnesses regarding these products have been reported to date.

      The recalled lots include 1356300 (exp. 01/2019), 1405700 (exp. 03/2019), 17A128 (exp. 03/2021) and W00103 (exp. 06/2019). The lot numbers can be found printed either on the bottom of the bottle or on the label. The white bottles contain capsules in quantities of either 60 or 90 capsules per bottle.

      The recalled product was sold online on the LL’s Magnetic Clay website and at brick and mortar retailers nationwide, and was also available through distributors other than LL’s Magnetic Clay that purchased the product from the same source.

      What to do

      Customers who purchased the recalled product should discontinue using it and return it to LL’s Magnetic Clay for a full refund.

      Consumers with questions may contact the company at 1-800-257-3315, Monday – Friday, 9am – 5pm.

      LL’s Magnetic Clay of Austin, Texas, is recalling certain lots of Prescript-Assist, a dietary supplement it marketed until late 2017.The product may co...
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