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. 2,446 recalls have been distributed to Washington in the last 12 months.

51,768 total recalls
2,446 in last 12 months

Showing 13611380 of 51,768 recalls

DrugSeptember 15, 2025· Graviti Pharmaceuticals Private Limited

Recalled Item: Bupropion Hydrochloride Extended-Release Tablets USP (XL) Recalled by...

The Issue: Failed Tablet/Capsule Specifications

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 15, 2025· Amerisource Health Services LLC

Recalled Item: Carbamazepine Extended-Release Tablets Recalled by Amerisource Health...

The Issue: Failed Dissolution Specifications.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceSeptember 12, 2025· Diagnostica Stago, Inc.

Recalled Item: Product: STA Liatest D-Di Recalled by Diagnostica Stago, Inc. Due to A...

The Issue: A potential risk of underestimation of D-Dimer (D-Di) levels with the two...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 12, 2025· Philips North America

Recalled Item: Cardiac Workstation 5000 Recalled by Philips North America Due to Failure of...

The Issue: Failure of Environmental Stress Testing from a pinched power module wire...

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

Class II — Potential Health HazardOngoing
DrugSeptember 12, 2025· JB Chemicals and Pharmaceuticals Ltd

Recalled Item: Cetirizine Hydrochloride Tablets USP 10 mg Recalled by JB Chemicals and...

The Issue: Tablet/Capsules Imprinted with Wrong ID

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

Class III — Low RiskOngoing
Refund
DrugSeptember 12, 2025· JB Chemicals and Pharmaceuticals Ltd

Recalled Item: Cetirizine Hydrochloride Tablets USP 10 mg Recalled by JB Chemicals and...

The Issue: Tablet/Capsules Imprinted with Wrong ID

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

Class III — Low RiskOngoing
Refund
DrugSeptember 12, 2025· The Harvard Drug Group LLC dba Major Pharmaceuticals and Rugby Laboratories

Recalled Item: Major ChlorproMAZINE Hydrochloride Tablets Recalled by The Harvard Drug...

The Issue: CGMP Deviations: Presence of N-Nitroso Desmethyl Chlorpromazine above the...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 12, 2025· The Harvard Drug Group LLC dba Major Pharmaceuticals and Rugby Laboratories

Recalled Item: Major ChlorproMAZINE Hydrochloride Tablets Recalled by The Harvard Drug...

The Issue: CGMP Deviations: Presence of N-Nitroso Desmethyl Chlorpromazine above the...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 12, 2025· The Harvard Drug Group LLC dba Major Pharmaceuticals and Rugby Laboratories

Recalled Item: Major ChlorproMAZINE Hydrochloride Tablets Recalled by The Harvard Drug...

The Issue: CGMP Deviations: Presence of N-Nitroso Desmethyl Chlorpromazine above the...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 12, 2025· The Harvard Drug Group LLC dba Major Pharmaceuticals and Rugby Laboratories

Recalled Item: Major ChlorproMAZINE Hydrochloride Tablets Recalled by The Harvard Drug...

The Issue: CGMP Deviations: Presence of N-Nitroso Desmethyl Chlorpromazine above the...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 12, 2025· The Harvard Drug Group LLC dba Major Pharmaceuticals and Rugby Laboratories

Recalled Item: Major ChlorproMAZINE Hydrochloride Tablets Recalled by The Harvard Drug...

The Issue: CGMP Deviations: Presence of N-Nitroso Desmethyl Chlorpromazine above the...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceSeptember 12, 2025· Philips North America

Recalled Item: Cardiac Workstation 7000 Recalled by Philips North America Due to Failure of...

The Issue: Failure of Environmental Stress Testing from a pinched power module wire...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 12, 2025· Argon Medical Devices, Inc

Recalled Item: Option"ELITE Vena Cava Filter System UDI-DI code: 00886333217151 Recalled by...

The Issue: Due to complaints of increased resistance when advancing the dilator within...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 11, 2025· Olympus Corporation of the Americas

Recalled Item: BRONCHOVIDEOSCOPE OLYMPUS BF-H1100 Recalled by Olympus Corporation of the...

The Issue: Additional IFU updates to provide further clarification on safe and...

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 11, 2025· Medline Industries, LP

Recalled Item: Excelsior Medical Recalled by Medline Industries, LP Due to Medline has...

The Issue: Medline has identified a limited quantity of saline IV flush syringes that...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 11, 2025· Olympus Corporation of the Americas

Recalled Item: BRONCHOVIDEOSCOPE OLYMPUS BF TYPE 1T150 Recalled by Olympus Corporation of...

The Issue: Additional IFU updates to provide further clarification on safe and...

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 11, 2025· Olympus Corporation of the Americas

Recalled Item: EVIS EXERA III BRONCHOVIDEOSCOPE OLYMPUS BF-Q190 Recalled by Olympus...

The Issue: Additional IFU updates to provide further clarification on safe and...

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 11, 2025· Boston Scientific Corporation

Recalled Item: LGX Preconnect with TENACIO Pump without InhibiZone Recalled by Boston...

The Issue: The potential for devices to experience inflation and/or deflation...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 11, 2025· Olympus Corporation of the Americas

Recalled Item: EVIS EXERA III BRONCHOVIDEOSCOPE OLYMPUS BF-H190 Recalled by Olympus...

The Issue: Additional IFU updates to provide further clarification on safe and...

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 11, 2025· Olympus Corporation of the Americas

Recalled Item: EVIS EXERA II BRONCHOVIDEOSCOPE OLYMPUS BF TYPE Q180-AC Recalled by Olympus...

The Issue: Additional IFU updates to provide further clarification on safe and...

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

Class I — Serious Health HazardOngoing