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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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