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. 2,765 recalls have been distributed to Washington in the last 12 months.

51,768 total recalls
2,765 in last 12 months

Showing 1510115120 of 51,768 recalls

FoodSeptember 30, 2021· Lake Wolf Creamery

Recalled Item: Lake Wolf Creamery Cheddar Curds Recalled by Lake Wolf Creamery Due to The...

The Issue: The milk pasteurization temperature was not recorded and/or the air space...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceSeptember 30, 2021· Mentor Texas, LP.

Recalled Item: MENTOR Saline-Filled Breast Implants are constructed from room temperature...

The Issue: Due to a manufacturing issue, Implant may have a potentially weakened area...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 29, 2021· Abbott Laboratories

Recalled Item: ARCHITECT i1000SR /1L86 and 1L87 Recalled by Abbott Laboratories Due to...

The Issue: Twelve software-related issues affecting software version 9.41 and earlier...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 29, 2021· Abbott Laboratories

Recalled Item: ARCHITECT c4000 /2P24 Recalled by Abbott Laboratories Due to Twelve...

The Issue: Twelve software-related issues affecting software version 9.41 and earlier...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 29, 2021· CooperSurgical, Inc.

Recalled Item: Quantum 2000 Electrosurgical Generators Cooper Surgical Part Number: 909075...

The Issue: Coagulate function may not operate with the use of the Hand Switch, failure...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 29, 2021· CooperSurgical, Inc.

Recalled Item: LEEP PRECISION Integrated System Recalled by CooperSurgical, Inc. Due to...

The Issue: Coagulate function may not operate with the use of the Hand Switch, failure...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 29, 2021· CooperSurgical, Inc.

Recalled Item: Quantum 2000 Electrosurgical Generators Cooper Surgical Part Number:...

The Issue: XXX

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 29, 2021· CooperSurgical, Inc.

Recalled Item: LEEP PRECISION Generator 220V Cooper Surgical Part Number: LP-20-220...

The Issue: Coagulate function may not operate with the use of the Hand Switch, failure...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 29, 2021· CooperSurgical, Inc.

Recalled Item: LEEP PRECISION Integrated System Recalled by CooperSurgical, Inc. Due to...

The Issue: Coagulate function may not operate with the use of the Hand Switch, failure...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 29, 2021· CooperSurgical, Inc.

Recalled Item: Quantum 2000 Electrosurgical Generators Cooper Surgical Part Number:...

The Issue: Coagulate function may not operate with the use of the Hand Switch, failure...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 29, 2021· CooperSurgical, Inc.

Recalled Item: LEEP PRECISION Generator 120V Cooper Surgical Part Number: LP-20-120...

The Issue: Coagulate function may not operate with the use of the Hand Switch, failure...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 29, 2021· Baxter Healthcare Corporation

Recalled Item: Hemodialysis Delivery System Recalled by Baxter Healthcare Corporation Due...

The Issue: If the operator initiates therapy with a saved prescription profile and...

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

Class II — Potential Health HazardOngoing
DrugSeptember 28, 2021· Revive Personal Products Company

Recalled Item: The Natural Dentist Healthy Balance Peppermint Sage Recalled by Revive...

The Issue: Labeling; Label mix-up and Wrong Bar Code; back label incorrectly states...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 28, 2021· Bryant Ranch Prepack, Inc. dba BRP Pharmaceuticals

Recalled Item: Butalbital Recalled by Bryant Ranch Prepack, Inc. dba BRP Pharmaceuticals...

The Issue: Labeling: Not Elsewhere Classified: the controlled substance classification...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugSeptember 28, 2021· Bryant Ranch Prepack, Inc. dba BRP Pharmaceuticals

Recalled Item: Butalbital Recalled by Bryant Ranch Prepack, Inc. dba BRP Pharmaceuticals...

The Issue: Labeling: Not Elsewhere Classified: the controlled substance classification...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
Medical DeviceSeptember 28, 2021· Cook Inc.

Recalled Item: Flexor Check-Flo Introducer - Raabe Modification Recalled by Cook Inc. Due...

The Issue: Affected lots may be manufactured incorrectly with the radiopaque marker...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 28, 2021· Cook Inc.

Recalled Item: Flexor Check-Flo Introducer Recalled by Cook Inc. Due to Affected lots may...

The Issue: Affected lots may be manufactured incorrectly with the radiopaque marker...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 28, 2021· Siemens Healthcare Diagnostics, Inc

Recalled Item: Atellica IM 1600 Analyzer Recalled by Siemens Healthcare Diagnostics, Inc...

The Issue: Ancillary reagent packs used on Atellica IM 1300 and Atellica IM 1600...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 28, 2021· Siemens Healthcare Diagnostics, Inc

Recalled Item: Atellica IM 1300 Analyzer Recalled by Siemens Healthcare Diagnostics, Inc...

The Issue: Ancillary reagent packs used on Atellica IM 1300 and Atellica IM 1600...

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

Class II — Potential Health HazardOngoing
DrugSeptember 27, 2021· Strides Pharma Inc.

Recalled Item: Potassium Chloride Extended-Release Tablets Recalled by Strides Pharma Inc....

The Issue: Failed Dissolution Specifications

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund