Product Recalls in Washington

Product recalls affecting Washington — including food, drugs, consumer products, medical devices, and vehicles distributed to Washington. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,592 recalls have been distributed to Washington in the last 12 months.

51,768 total recalls
2,592 in last 12 months

Showing 3768137700 of 51,768 recalls

Medical DeviceNovember 16, 2015· Ameditech Inc

Recalled Item: iCup DX 11 Panel w/ Adulterant Recalled by Ameditech Inc Due to Ameditechs...

The Issue: Ameditechs Drugs of Abuse Tests listed above have shown reduced reactivity...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class III — Low RiskOngoing
Medical DeviceNovember 16, 2015· Ameditech Inc

Recalled Item: DrugSmart 9 Test Cup (BUP) Recalled by Ameditech Inc Due to Ameditechs Drugs...

The Issue: Ameditechs Drugs of Abuse Tests listed above have shown reduced reactivity...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class III — Low RiskOngoing
Medical DeviceNovember 16, 2015· Ameditech Inc

Recalled Item: ProScreen CLIA Waived Cup 6 Drugs w/Adul Recalled by Ameditech Inc Due to...

The Issue: Ameditechs Drugs of Abuse Tests listed above have shown reduced reactivity...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class III — Low RiskOngoing
Medical DeviceNovember 16, 2015· Ameditech Inc

Recalled Item: 6 Panel Cup Body and Lid w/Adult (AU) Recalled by Ameditech Inc Due to...

The Issue: Ameditechs Drugs of Abuse Tests listed above have shown reduced reactivity...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class III — Low RiskOngoing
Medical DeviceNovember 16, 2015· Ameditech Inc

Recalled Item: EDI BZO Uncut Sheet - Cup* Recalled by Ameditech Inc Due to Ameditechs Drugs...

The Issue: Ameditechs Drugs of Abuse Tests listed above have shown reduced reactivity...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class III — Low RiskOngoing
Medical DeviceNovember 16, 2015· Ameditech Inc

Recalled Item: ProScreen 6 Panel Cassette w/Adult (AU) Recalled by Ameditech Inc Due to...

The Issue: Ameditechs Drugs of Abuse Tests listed above have shown reduced reactivity...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class III — Low RiskOngoing
Medical DeviceNovember 16, 2015· Nephron Pharmaceuticals Corp.

Recalled Item: Sodium Chloride Inhalation Solution Recalled by Nephron Pharmaceuticals...

The Issue: Lack of Assurance of Sterility: Internal dye ingress test failure to assure...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 16, 2015· Nephron Pharmaceuticals Corp.

Recalled Item: Sodium Chloride Inhalation Solution Recalled by Nephron Pharmaceuticals...

The Issue: Lack of Assurance of Sterility: Internal dye ingress test failure to assure...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 13, 2015· GE Medical Systems, LLC

Recalled Item: GE Healthcare Optima CL323i Product Usage: The angiographic X-ray systems...

The Issue: GE Healthcare has recently become aware of a potential safety issue related...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 13, 2015· Maquet Cardiovascular Us Sales, Llc

Recalled Item: Maquet HCU 30 Coolant Type R134A Filling weight 250 g Recalled by Maquet...

The Issue: Failure of the HEATER-COOLER UNIT (HCU 30) Type 2 power supply board. A drop...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 13, 2015· STERILMED, INC.

Recalled Item: Zimmer Recalled by STERILMED, INC. Due to Sterilmed, Inc. is voluntarily...

The Issue: Sterilmed, Inc. is voluntarily recalling all unexpired Reprocessed...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 13, 2015· GE Medical Systems, LLC

Recalled Item: GE Healthcare Optima IGS 320. Product Usage: The angiographic X-ray Recalled...

The Issue: GE Healthcare has recently become aware of a potential safety issue related...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
FoodNovember 13, 2015· A. L. Schutzman Company, Inc.

Recalled Item: Honey Mustard Pretzel Mix sold under the following brand and size: Girl...

The Issue: The honey mustard pretzel mix lists whey in the ingredient list but does not...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodNovember 13, 2015· A. L. Schutzman Company, Inc.

Recalled Item: Honey Mustard Mix sold under the following brand: Ashdon Farms Recalled by...

The Issue: The honey mustard mix lists whey in the ingredient list but does not list...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodNovember 12, 2015· Campbell Soup Supply Co., LLC

Recalled Item: Campbell's SpaghettiOs Original Pasta in Tomato and Cheese Sauce Net...

The Issue: Potential choking hazard posed by pieces of red plastic found in cans.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodNovember 12, 2015· Trader Joes Company

Recalled Item: Butternut Squash Triangoli Recalled by Trader Joes Company Due to Undeclared...

The Issue: Trader Joe's is recalling Trader Giotto's Butternut Squash Triangoli because...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
Medical DeviceNovember 12, 2015· Corflex

Recalled Item: CONTENDER POST-OP-KNEE BRACE FULL FOAM Model: 75-7550-000 Post-Operative...

The Issue: Knee brace could fail to maintain the locked position and a loss of balance...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 12, 2015· Bestmed, LLC

Recalled Item: Digital Temple Thermometer labeled under: Bestmed Recalled by Bestmed, LLC...

The Issue: An incorrect calibration of the thermometer that causes the device to...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 12, 2015· Corflex

Recalled Item: ORTHO SPEC GRP CONTENDER POST-OP-KNEE BRACE LITE Model: 75-7500-075...

The Issue: Knee brace could fail to maintain the locked position and a loss of balance...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 12, 2015· Corflex

Recalled Item: Corflex Contender Post-Op Knee Brace Lite Model: 75-7500-000 Post-Operative...

The Issue: Knee brace could fail to maintain the locked position and a loss of balance...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing