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. 2,824 recalls have been distributed to Washington in the last 12 months.

51,768 total recalls
2,824 in last 12 months

Showing 38613880 of 51,768 recalls

DrugNovember 26, 2024· Curium US, LLC

Recalled Item: Kit for the Preparation of Technetium Tc 99m Sestamibi Injection Recalled by...

The Issue: Lack of Assurance of Sterility; Improper crimps on vials impacting the...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceNovember 26, 2024· O&M HALYARD, INC.

Recalled Item: Brand Name: HALYARD Product Name: Laparotomy Pack Model/Catalog Number:...

The Issue: Elevated residues of anti-block/slip additive used in manufacturing found...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 26, 2024· Beckman Coulter, Inc.

Recalled Item: Access Intact PTH assay Recalled by Beckman Coulter, Inc. Due to Beckman...

The Issue: Beckman Coulter has identified that some Access PTH reagent packs from lot...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 26, 2024· Applied Medical Technology Inc

Recalled Item: AMT Mini Enteral Extension Set Recalled by Applied Medical Technology Inc...

The Issue: The extension sets subject to this recall have ENFit connections, although...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 26, 2024· 3M Unitek Corporation

Recalled Item: 3M Unitek Transbond Plus Self-Etching Primer (100 unit Recalled by 3M Unitek...

The Issue: Due to an increase of complaints for bracket bond failures and skin...

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

Class II — Potential Health HazardOngoing
DrugNovember 25, 2024· Macleods Pharmaceuticals Ltd

Recalled Item: Olanzapine Tablets Recalled by Macleods Pharmaceuticals Ltd Due to Failed...

The Issue: Failed Impurities/Degradation Specifications

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceNovember 25, 2024· Olympus Corporation of the Americas

Recalled Item: Brand Name: Olympus Thunderbeat Front-Actuated Grip Type S Hand Instrument...

The Issue: The probe tips of the hand instruments are being damaged or breaking...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 25, 2024· Olympus Corporation of the Americas

Recalled Item: Brand Name: Olympus Thunderbeat Front-Actuated Grip Type S Hand Instrument...

The Issue: The probe tips of the hand instruments are being damaged or breaking...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 25, 2024· Olympus Corporation of the Americas

Recalled Item: Brand Name: Olympus Thunderbeat Front-Actuated Grip Type S Hand Instrument...

The Issue: The probe tips of the hand instruments are being damaged or breaking...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 25, 2024· Olympus Corporation of the Americas

Recalled Item: Brand Name: Olympus Thunderbeat Front-Actuated Grip Type S Hand Instrument...

The Issue: The probe tips of the hand instruments are being damaged or breaking...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 25, 2024· Olympus Corporation of the Americas

Recalled Item: Brand Name: Olympus Thunderbeat Front-Actuated Grip Type S Hand Instrument...

The Issue: The probe tips of the hand instruments are being damaged or breaking...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 25, 2024· Olympus Corporation of the Americas

Recalled Item: Brand Name: Olympus Thunderbeat Front-Actuated Grip Type S Hand Instrument...

The Issue: The probe tips of the hand instruments are being damaged or breaking...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 25, 2024· Olympus Corporation of the Americas

Recalled Item: Brand Name: Olympus Thunderbeat Front-Actuated Grip Type S Hand Instrument...

The Issue: The probe tips of the hand instruments are being damaged or breaking...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 25, 2024· Olympus Corporation of the Americas

Recalled Item: Brand Name: Olympus Thunderbeat Front-Actuated Grip Type S Hand Instrument...

The Issue: The probe tips of the hand instruments are being damaged or breaking...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 25, 2024· Olympus Corporation of the Americas

Recalled Item: Brand Name: Olympus Thunderbeat Front-Actuated Grip Type S Hand Instrument...

The Issue: The probe tips of the hand instruments are being damaged or breaking...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 25, 2024· Olympus Corporation of the Americas

Recalled Item: Brand Name: Olympus Thunderbeat Front-Actuated Grip Type S Hand Instrument...

The Issue: The probe tips of the hand instruments are being damaged or breaking...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 25, 2024· Olympus Corporation of the Americas

Recalled Item: Brand Name: Olympus Thunderbeat Front-Actuated Grip Type S Hand Instrument...

The Issue: The probe tips of the hand instruments are being damaged or breaking...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 25, 2024· Angiodynamics, Inc.

Recalled Item: AURYON LASER SYSTEM 100-120 VAC. Model Number: EXM001. Product Number:...

The Issue: Potential for procedural delays or interruptions during use of the Auryon...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 25, 2024· Spacelabs Healthcare, Inc.

Recalled Item: Xhibit Telemetry Receiver Recalled by Spacelabs Healthcare, Inc. Due to...

The Issue: Telemetry receiver systems may experience a Windows proxy Issue causing the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 25, 2024· Spacelabs Healthcare, Inc.

Recalled Item: Xhibit Telemetry Receiver with Software Recalled by Spacelabs Healthcare,...

The Issue: Telemetry receivers with affected software versions may experience...

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

Class II — Potential Health HazardOngoing