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    Flying Tiger Copenhagen recalls crocodile candleholders

    The candleholders are flammable and can catch fire

    Flying Tiger of Copenhagen, Denmark, is recalling about 180 crocodile candleholders.

    The candleholders are flammable and can catch fire, posing a fire hazard when the candle burns down.

    The company has received one report of the candleholder catching fire. No injuries have been reported.

    This recall involves Flying Tiger Copenhagen candleholders shaped as a gold-colored crocodile. The candleholders measure 7 inches long by 2 inches wide. The candle holder is inside the crocodile’s wide open mouth.

    A hangtag attached to the holder reads, “Lysestage – Candle holder” and on the back “Item # 3017653, Batch # 218377”

    The candleholders, manufactured in China, were sold at Flying Tiger Copenhagen stores nationwide from September 2019, through October 2019, for about $4.

    What to do

    Consumer should immediately stop using the recalled candleholders and contact Flying Tiger for a full refund.

    Consumers may contact Flying Tiger Copenhagen toll-free at (844) 350-0560 from 8 a.m. to 5 p.m. (ET) Monday through Friday, by email at info.us@flyingtiger.com or online at www.flyingtiger.com and click on “Product Information” at the bottom of the page more information.

    Flying Tiger of Copenhagen, Denmark, is recalling about 180 crocodile candleholders.The candleholders are flammable and can catch fire, posing a fire h...
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    American Health Packaging recalls Ranitidine Syrup

    The medication is contaminated with a probable cancer-causer

    American Health Packaging is recalling eight lots of Ranitidine Syrup.

    The product is contaminated with N-Nitrosodimethylamine (NDMA), a probable human carcinogen, above levels established by the FDA.

    The recalled product is used as a short-term treatment for active duodenal ulcers, maintenance therapy for duodenal ulcer patients, treatment of pathological hypersecretory conditions, short-term treatment of active, benign gastric ulcers, maintenance therapy for gastric ulcers, treatment of GERD and treatment of endoscopically diagnosed erosive esophagitis.

    The following product, which was distributed nationwide to wholesalers for use in hospital settings, is being recalled:

    Product DescriptionAHP Lot No.Expiration Date
    AHP Ranitidine Syrup (Ranitidine Oral Solution USP) 150 mg/10 mL Liquid Unit Dose Cups
    Case NDC#: 60687-260-23
    (Individual Dose NDC: 60687-260-42)
    18372310/31/2020
    18427810/31/2020
    18765205/31/2021
    AHP Ranitidine Syrup (Ranitidine Oral Solution USP) 150 mg/10 mL Liquid Unit Dose Cups
    Case NDC#: 60687-260-69
    (Individual Dose NDC: 60687-260-42)
    17787401/31/2020
    17841302/29/2020
    18344910/31/2020
    18444512/31/2020
    18656303/31/2021

    What to do

    Patients should contact their physician or healthcare provider if they have experienced any problems that may be related to taking or using this product.

    Consumers with questions may contact Inmar Pharmaceuticals Services at (800) 967-5952 (option 1) from 9:00am – 5:00pm (EST) Monday thru Friday.

    American Health Packaging is recalling eight lots of Ranitidine Syrup.The product is contaminated with N-Nitrosodimethylamine (NDMA), a probable human...
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    Med Man Recalls Up2

    The dietary supplement contains sildenafil rendering it an unapproved drug

    Med Man Distribution is recalling all lots of Up2 dietary supplement.

    The product, marketed as an “all-natural libido for men and women,” is tainted with sildenafil, making it an unapproved drug for which safety and efficacy have not been established.

    The firm says it has not received any reports of adverse events.

    Lots of the recalled product include 240 ten-count units, UPC 85606300322, 480 four-count packages, UPC 856063006315, and 960 singlepack units, UPC856063006308.

    It was sold in the U.S. to Regal Labs and their retailers.

    What to do

    Med Man is notifying its distributors and their customers by email and is arranging for destruction of all recalled products.

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

    Consumers with questions may contact Med Man at (705) 297-5321 Monday – Friday, 9 am – 5pm (ET) or by email at dirtyderek669@gmail.com.

    Med Man Distribution is recalling all lots of Up2 dietary supplement.The product, marketed as an “all-natural libido for men and women,” is tainted wit...
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      Kenmore microwave ovens recalled

      The microwave’s exterior could reach excessively high temperatures

      Sears Holdings Management Corporation of Hoffman Estates, Ill., is recalling about 700 Kenmore Elite microwave ovens.

      Incorrect wiring causes the microwave’s exterior to reach temperatures exceeding 183 degrees Fahrenheit, posing a burn hazard.

      No incidents or injuries are reported.

      This recall involves 1,000-watt countertop convection microwave ovens manufactured under the Kenmore Elite brand name on April 27, 2017. This manufacturing date of the recalled microwave ovens is identifiable by the first six digits of their serial numbers, each of which begins with the numerals “170427”.

      The model number of the recalled microwaves is “204.77603610”. The brand name, model number and serial number can be found on the data plate on the back of the microwave ovens.

      The brand name is printed near the bottom of the door.

      Model Number

          Serial Number Range

      204.77603610

          17042700001 

      and 17042700684

      The microwave ovens, manufactured in China, were sold exclusively at Sears and Sears Hometown and Outlet Stores nationwide from May 2017, through July 2018, for about $350.

      What to do

      Consumers should immediately stop using the recalled microwave ovens and contact Sears for a free in-home repair.

      Consumers may contact Sears at (800) 659-7026 from 7 a.m. to 7 p.m. (CT) Monday through Friday, or online at www.sears.com and click on “Product Recalls” at the bottom of the page for more information.

      Sears Holdings Management Corporation of Hoffman Estates, Ill., is recalling about 700 Kenmore Elite microwave ovens.Incorrect wiring causes the microw...
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      You Chang Trading recalls Tilapia filets

      The product was not inspected upon being imported into the U.S.

      You Chang Trading of Brooklyn, N.Y., is recalling an undetermined amount of raw Tilapia filets.

      The product was not inspected upon being imported into the U.S.

      There are no confirmed reports of adverse reactions.

      The following frozen, raw item, produced between November 13, 2018, and January 5, 2019, is being recalled:

      • 22-lb. white cardboard boxes containing “CONWAY TILAPIA FILLETS PRODUCT OF HONGKONG” and lot codes 20181113, 20181203, or 20190105 and sell by dates of 11/16/2020, 12/03/2020, or 01/05/2021 represented on the label.

      The recalled product was shipped to distributor and retail locations in Massachusetts, New Jersey, New York and Pennsylvania.

      What to do

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

      Consumers with questions may contact Yang Zhou Lu at (718) 633-7816.

      You Chang Trading of Brooklyn, N.Y., is recalling an undetermined amount of raw Tilapia filets.The product was not inspected upon being imported into t...
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      Quest Products recalls ALOCANE Emergency Burn Pads

      The packaging is not child resistant as required by law

      Quest Products of Pleasant Prairie, Wis., is recalling 153,000 packages of ALOCANE Emergency Burn Pads.

      The packaging is not child resistant as required by the Poison Prevention Packaging Act. The pads contain lidocaine, posing a risk of poisoning to young children if they were to place the pad in their mouth.

      No incidents or injuries are reported.

      This recall involves ALOCANE Emergency Burn Pads (10-count and 15-count) which come in a white and red box with “MAXIMUM STRENGTH ALOCANE Emergency Burn Pads” printed on the front.

      The product is an over the counter Gel Infused Pad with lidocaine (4%) as the active ingredient the lot numbers 4179, 4180, 4235, 4645, 4646 or 4698 printed next to the barcode on the box.

      The UPC number for the affected product is 8-46241-02448-7 and is located on the bottom of the box.

      The pads, manufactured in the U.S., were sold at Walgreens, Walmart, Target, Kroger, Meijer, other pharmacies nationwide, and online at Amazon.com, HomeDepot.com, Overstock.com, MyQuestStore.com and Alocane.com from March 2018, through June 2019, for about $9.

      What to do

      Consumers should immediately stop using the recalled burn pads, store them in a safe location out of reach of children and contact Quest Products to return the pain relieving pads for a free ALOCANE Emergency Burn Gel 2.5 ounce child resistant tube or a full refund.

      Consumers may contact Quest Products at (800) 650-0113 from 9 a.m. to 5 p.m. (CT) Monday through Friday, or online at www.alocane.com and click on “Contact Us” at the bottom of the page for more information.

      Quest Products of Pleasant Prairie, Wis., is recalling 153,000 packages of ALOCANE Emergency Burn Pads.The packaging is not child resistant as required...
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      Forest River recalls Dynamax DX3 and Force motorhomes

      The front axle stabilizer bracket may break

      Forest River is recalling 14 model year 2017 Dynamax DX3 and Force motorhomes.

      The front axle stabilizer bracket may not properly mount to the axle, and may break as a result.

      If the stabilizer bracket breaks, a sudden loss of vehicle control could occur, increasing the risk of a crash.

      What to do

      Forest River has notified owners, and a Detroit Diesel dealer will perform the recall remedy.

      The stabilizer brackets and I-beams will be inspected and spacers and replacement stabilizer brackets will be installed, as necessary, free of charge.

      The recall began November 6, 2019.

      Owners may contact Forest River customer service at (800) 348-7440 or find a Detroit Diesel location at www.detroitdiesel.com/locations/default.aspx.

      Forest River's number for this recall is 55-1105.

      Forest River is recalling 14 model year 2017 Dynamax DX3 and Force motorhomes.The front axle stabilizer bracket may not properly mount to the axle, and...
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      Aurobindo recalls Ranitidine tablets, capsules and syrup

      The medications are contaminated with a probable cancer-causer

      Aurobindo Pharma USA is recalling one lot of Ranitidine tablets, 37 lots of Ranitidine capsules and Ranitidine syrup.

      The products, used to treat heartburn associated with acid indigestion and sour stomach brought on by eating or drinking certain foods and beverages, are contaminated with N-Nitrosodimethylamine (NDMA), a probable human carcinogen, above levels established by the FDA.

      The firm as not received any reports of adverse events to date.

      The following products, which are packaged in bottles, are being recalled:

      Product NameNDCBatch NumberExp. Date
      Ranitidine Tablets 150mg55910-092-79NBSB19001DA3Feb-2021
      Ranitidine Capsules 150mg59651-144-60RA1518001-AJul-2020
      RA1518002-AJul-2020
      59651-144-05RA1518002-BJul-2020
      RA1518003-AJul-2020
      RA1518004-AAug-2020
      RA1518005-AAug-2020
      59651-144-60RA1518005-BAug-2020
      RA1518006-AAug-2020
      59651-144-05RA1518007-ASep 2020
      RA1518008-ASep 2020
      RA1518009-ASep 2020
      RA1518010-AOct 2020
      RA1518011-ANov 2020
      RA1518012-ANov 2020
      RA1518013-ANov 2020
      RA1518014-ANov 2020
      RA1518015-ANov 2020
      59651-144-60RA1519003-AMay-2021
      59651-144-05RA1519003-BMay 2021
      RA1519004-AMay 2021
      Ranitidine Capsules 300mg59651-145-30RA3018001-AJul-2020
      RA3018002-AJul-2020
      RA3018003-AJul-2020
      RA3018004-AAug-2020
      RA3018005-AAug-2020
      RA3018006-AAug-2020
      RA3018007-ASep-2020
      RA3018008-ASep-2020
      RA3018009-ASep-2020
      RA3018010-AOct-2020
      RA3019001-AJan 2021
      RA3019002-AJan 2021
      RA3019003-AMay-2021
      Ranitidine Syrup (Ranitidine Oral Solution, USP)  15 mg/mL (75 mg/5 mL)65862-431-74UI1519001-AMay-2021
      UI1519002-AMay-2021
      UI1519003-AMay-2021
      UI1519004-AMay-2021

      The recalled products can be identified by checking the product name, manufacturer details and batch or lot number on the bottle containing these products.

      They were distributed nationwide to Aurobindo Pharma USA, Inc. and AuroHealth wholesale and distributor customers from September 28, 2018, through September 19, 2019.

      What to do

      Patients should continue taking their medication and contact their pharmacist or physician who can advise them about an alternative treatment prior to returning their medication.

      Consumers with questions regarding the return of this product may contact Qualanex at (888) 504-2014 from 7:00 am to 4:00 pm (CST) Monday – Friday or by email at recall@qualanex.com.

      Aurobindo Pharma USA is recalling one lot of Ranitidine tablets, 37 lots of Ranitidine capsules and Ranitidine syrup.The products, used to treat heartb...
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      H&H Sports recalls VCAN V531 motorcycle helmets

      The helmet may separate from the wearer's head in a crash

      H&H Sports Protection is recalling 4,218 VCAN V531 motorcycle helmets in sizes XS, S, M, L, XL, and XXL, sold exclusively through Amazon.

      The helmet retention system may fail, allowing the helmet to separate from the wearer's head in a crash.

      A helmet that doesn't stay secured to the head can increase the risk of injury.

      What to do

      Amazon will notify the helmet purchasers and instruct them to return the helmets for a full refund.

      The recall is expected to begin in November 2019.

      Owners may contact H&H Sports at (626) 444-0107.

      H&H; Sports Protection is recalling 4,218 VCAN V531 motorcycle helmets in sizes XS, S, M, L, XL, and XXL, sold exclusively through Amazon.The helmet re...
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      Mystery Ranch recalls semi-automatic handgun holsters

      The retention strap can disconnect from the holster, allowing the handgun to fall

      Mystery Ranch of Bozeman, Mont., is recalling about 500 Quick Draw Side Arm Holster – Semi-Auto.

      The retention strap can disconnect from the holster and allow the handgun to fall. If this this happens, the gun can unexpectedly discharge, posing a serious injury risk.

      The firm has received 42 reports of the strap disconnecting from the holster, including one report of the gun unexpectedly coming out of a holster. No injuries have been reported.

      This recall involves the Mystery Ranch Quick Draw Side Arm Holster – Semi-Auto holsters designed to be used with semi-automatic firearms.

      The holsters have a camel hypalon exterior, foam cushioning and a snap closure.

      Mystery Ranch; Date on Tracking Tag: 28 May, 2019; Bundle No.: 294411; Line: S-B and Inspection: M-V are printed on the tracking tag inside of the recalled holster. UPC number 888564163139 is printed on the packaging.

      The holsters, manufactured in the Philippines, were sold at Al’s Sporting Goods, Archery Country, Bering’s, Bink’s Outfitters, Bull Basin Archery, Capital Sports, Farwest Sports, Gardenswartz Sporting Goods Archery, Pappas Trading Post, Rusted Moon Outfitters, Scheels, Shedhorn Sports, Trail Head Montana, and Wind River Outdoor Company nationwide and online at Al’s Sporting Goods, Archery Country, Bering’s, goHUNT.com, Mountain Archery, MysteryRanch.com, Scheels, Schnee’s, Shedhorn Sports, and TacticalGear.com from August 2019, through October 2019, for about $25.

      What to do

      Consumers should immediately stop using the recalled holsters and contact Mystery Ranch for a full refund. The firm is contacting all known purchasers directly.

      Consumers may contact Mystery Ranch toll-free at (833) 548-1999 from 9 a.m. to 5 p.m. (MT) Monday through Friday, by e-mail at customerservice@mysteryranch.com or online at www.mysteryranch.com and click on “Product Recalls” at the bottom of the page for more information

      Mystery Ranch of Bozeman, Mont., is recalling about 500 Quick Draw Side Arm Holster – Semi-Auto.The retention strap can disconnect from the holster and...
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      Forest River recalls EVO, Salem and Wildwood travel trailers

      The cooktops were installed with an improper liquid propane gas line

      Forest River is recalling 41 model year 2020 EVO, Salem and Wildwood travel trailers.

      The trailer cooktops were installed with a rubber liquid propane (LP) gas line instead of a copper one.

      The rubber hose may melt, allowing gas to enter the vehicle, increasing the risk of a fire.

      What to do

      Forest River has notified owners, and dealers will replace the rubber LP gas line with a copper gas line free of charge.

      The recall began November 7, 2019.

      Owners may contact Forest River customer service at (909) 873-3777. Forest River's number for this recall is 67A-1107.

      Forest River is recalling 41 model year 2020 EVO, Salem and Wildwood travel trailers.The trailer cooktops were installed with a rubber liquid propane (...
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      Mill Stream Corp. recalls Cold Smoked Salmon

      The product may be contaminated with Clostridium botulinum

      Mill Stream Corp. (Sullivan Harbor Farm) of Hancock, Maine, is recalling ten lots of Cold Smoked Salmon.

      The product may be contaminated with Clostridium botulinum, which can cause life-threatening illness or death.

      No illnesses have been reported to date.

      The recalled product, sold between March 6, 2019, and September 17, 2019, in vacuum sealed packages in the following sizes: whole salmon side, 2 lb., 1 lb., 8 oz., and 4 oz., is marked with the following lot numbers marked on the back of the packages: 7049, 7050, 7051, 7052, 7054, 7056, 7058, 7060, 7062, 7066.

      It was sold and distributed through retail, wholesale and online orders in Maine, Massachusetts, Vermont, Rhode Island, New York, Connecticut, Pennsylvania, New Jersey, Ohio, Utah, Iowa, Tennessee, Minnesota, Colorado, Florida, Arizona, Wisconsin, Washington, Georgia, Illinois, Virginia, Michigan and Texas.

      What to do

      Customers who purchased the product should not use the product even if it does not look or smell spoiled, but discard it immediately.

      Consumers with questions may contact the company at (207) 266-0621 Monday – Friday, 8am – 5pm (EST).

      Mill Stream Corp. (Sullivan Harbor Farm) of Hancock, Maine, is recalling ten lots of Cold Smoked Salmon.The product may be contaminated with Clostridiu...
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      Keystone recalls model year 2020 Dutchmen Atlas trailers

      The trailer may have an improper propane supply hose

      Keystone RV Company is recalling five model year 2020 Dutchmen Atlas 3382BH trailers.

      The trailers may have a non-metallic propane supply hose installed inside the burner box of the cooktop, instead of a copper supply hose.

      Under certain conditions, the heat from the range burner may cause the hose to melt and leak propane, increasing the risk of a fire or an injury.

      What to do

      Keystone will notify owners, and dealers will remove the non-metallic propane gas line and attach it to a copper propane gas line free of charge.

      The recall is expected to begin November 15, 2019.

      Owners may contact Keystone customer service at (866) 425-4369. Keystone's number for this recall is 19-363.

      Keystone RV Company is recalling five model year 2020 Dutchmen Atlas 3382BH trailers.The trailers may have a non-metallic propane supply hose installed...
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      Jayco recalls model year 2017 Pinnacle Fifth Wheel trailers

      The suspension system may fail

      Jayco is recalling 908 model year 2017 Pinnacle Fifth Wheel trailers.

      The vehicle's suspension may allow the tires to contact the structure when under a certain load, which can cause damage to the tires.

      If the tire becomes damaged, causing premature tire wear, it can cause loss of vehicle control and increase the risk of a crash.

      What to do

      Jayco will notify owners, and dealers will inspect the condition of the leaf spring, rubber equalizer and bump stop clearance, and provide replacement of the leave spring or rubber equalizer if necessary. This repair will be done free of charge.

      The recall is expected to begin December 2, 2019.

      Owners may contact Jayco customer service at (800) 517-9137. Jayco's number for this recall is 9901443.

      Jayco is recalling 908 model year 2017 Pinnacle Fifth Wheel trailers.The vehicle's suspension may allow the tires to contact the structure when under a...
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      Airstream recalls model year 2019-2020 Atlas motorhomes

      Some of the 12V circuits may have insufficient overcurrent protection

      Airstream is recalling 151 model year 2019-2020 Atlas motorhomes.

      The SH1 Breaker Terminal may be wired incorrectly, causing some of the 12V circuits to have insufficient overcurrent protection.

      Incorrectly fused wires may overheat, increasing the risk of a fire.

      What to do

      Airstream will notify owners, and dealers will correct the wiring, as necessary, free of charge.

      The recall is expected to begin December 14, 2019.

      Owners may contact Airstream customer service at (877) 596-6505 or (937) 596-6111, extension 7401 or 7411.

      Airstream is recalling 151 model year 2019-2020 Atlas motorhomes.The SH1 Breaker Terminal may be wired incorrectly, causing some of the 12V circuits to...
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      Padrino Foods recalls beef tamales

      The products are labeled as beef and sirloin tamales but contain pork

      Padrino Foods of Irving, Texas, is recalling approximately 1,931 pounds of beef tamales.

      Although the products are labeled as beef and sirloin tamales, they actually contain pork.

      There are no confirmed reports of adverse reactions.

      The following fully-cooked, not shelf-stable items, produced on May 8, 2019, are being recalled:

      • 60-oz. packages containing “padrino foods BEEF & SIRLOIN TAMALES Homestyle in corn husks” with lot code 2128903 and a sell-by date 12-27-19.

      The recall products, bearing establishment number “EST. 13136” inside the USDA mark of inspection, were sold at retail locations in Kansas, Louisiana, Oklahoma and Texas.

      What to do

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

      Consumers with questions may contact Diane Luther at (214) 905-3444.

      Padrino Foods of Irving, Texas, is recalling approximately 1,931 pounds of beef tamales.Although the products are labeled as beef and sirloin tamales,...
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      Indian recalls Chief, Chieftain, Roadmaster and Springfield motorcycles

      The gear position display may show the motorcycle is in neutral when it is actually in gear

      Indian Motorcycle Company is recalling 52,745 model year 2014-2019 Chief, Chieftain, Roadmaster and Springfield motorcycles.

      The gear position switch contacts may oxidize, causing the gear position display to inaccurately show that the motorcycle is in neutral when it is actually in gear.

      If the transmission is not in neutral when the motorcycle is started, the motorcycle may move unexpectedly, increasing the risk of a crash.

      What to do

      Indian will notify owners, and -- as an interim repair -- dealers will clean the gear position switch. The switch will be replaced, once parts are available, currently expected to be in the first few months of 2020. These repairs will be performed free of charge.

      Interim letters notifying owners of the safety risk will be mailed November 19, 2019.

      Owners may contact Indian customer service at (877) 204-3697. Indian's number for this recall is I-19-03.

      Indian Motorcycle Company is recalling 52,745 model year 2014-2019 Chief, Chieftain, Roadmaster and Springfield motorcycles.The gear position switch co...
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      Skylight recalls power adapters

      The casing can break when plugged into an electrical outlet

      Skylight of San Francisco, Calif., is recalling about 65,000 Series I power adapters for Skylight digital photo frames sold in the U.S., and Canada.

      The power adapter casing can break when plugged into an electrical outlet, exposing its metal prongs, posing an electrical shock hazard.

      The firm has received eight reports of adapters breaking and exposing its metal prongs, including one report of an electric shock to a consumer.

      This recall involves the Series I power adapters sold with Skylight digital photo frames. The power adapters are black and have a circular indentation on the side. UPC code 679113611535 can be found on the packaging.

      Only the Series I adapters are included in this recall.

      The adapters, manufactured in China, were sold online at www.skylightframe.com and Amazon.com, and in Von Maur stores nationwide from April 2018, through March 2019, for about $160 with the digital photo frame.

      What to do

      Consumers should immediately stop using the recalled adapters and contact Skylight for instructions on proper disposal and how to receive a free replacement adapter. Skylight is contacting all known purchasers directly.

      Consumers may contact Skylight toll-free at (888) 359-4389 from 8 a.m. to 7 p.m. (ET) Monday through Friday, by email at newadapter@realtimeresults.net, or online at www.skylightframe.com and click on Product Recall Information at the bottom of the page for more information.

      Skylight of San Francisco, Calif., is recalling about 65,000 Series I power adapters for Skylight digital photo frames sold in the U.S., and Canada.The...
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