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. 2,820 recalls have been distributed to Washington in the last 12 months.

51,768 total recalls
2,820 in last 12 months

Showing 48814900 of 51,768 recalls

DrugAugust 12, 2024· FDC Limited

Recalled Item: Timolol Maleate Ophthalmic Solution USP Recalled by FDC Limited Due to...

The Issue: Defective Container: patients are unable to get the solution out of the...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceAugust 12, 2024· Merit Medical Systems, Inc.

Recalled Item: Custom Procedure Kit Recalled by Merit Medical Systems, Inc. Due to 7F...

The Issue: 7F sheath introducers labeled as 7.5F

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 12, 2024· Merit Medical Systems, Inc.

Recalled Item: Prelude Sheath Introducer 7.5F Recalled by Merit Medical Systems, Inc. Due...

The Issue: 7F sheath introducers labeled as 7.5F

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 12, 2024· SEER MEDICAL PTY LTD

Recalled Item: Seer Home System is an ambulatory electroencephalograph (EEG) system...

The Issue: During CAPA investigations of sight production inconsistencies, it was...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 12, 2024· Smith & Nephew Inc.

Recalled Item: ROTATION MEDICAL TENDON STAPLES (8) (narrow indication)-Intended for...

The Issue: Product packaging process may result in an improper or incomplete seal of...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 12, 2024· Smith & Nephew Inc.

Recalled Item: ROTATION MEDICAL TENDON STAPLES (8) (broad indication)-Intended for fixation...

The Issue: Product packaging process may result in an improper or incomplete seal of...

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

Class II — Potential Health HazardOngoing
FoodAugust 9, 2024· Prime Food Processing Corp.

Recalled Item: Prime Food brand Steam Bun with Egg Custard & Coconut Added Recalled by...

The Issue: Products may contain undeclared sesame

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

Class I — Serious Health HazardOngoing
Refund
FoodAugust 9, 2024· Prime Food Processing Corp.

Recalled Item: Prime Food brand Steam Bun with Egg Custard Added Recalled by Prime Food...

The Issue: Products may contain undeclared sesame

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

Class I — Serious Health HazardOngoing
Refund
DrugAugust 9, 2024· Direct Rx

Recalled Item: Ibuprofen 800mg Recalled by Direct Rx Due to Failed Impurities/Degradation...

The Issue: Failed Impurities/Degradation Specifications: Product failed impurity...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceAugust 9, 2024· Murata Vios, Inc.

Recalled Item: Vios Monitoring System Bedside Monitor Model BSM2050 Recalled by Murata...

The Issue: Batteries may deplete over time while not in use if devices are stored...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 9, 2024· Physio-Control, Inc.

Recalled Item: STERILIZABLE INTERNAL DEFIBRILLATION PADDLES STERILIZABLE INTERNAL...

The Issue: Due to customer complaints and out of box failures, the firm is conducting a...

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

Class II — Potential Health HazardOngoing
DrugAugust 8, 2024· Teva Pharmaceuticals USA, Inc

Recalled Item: Testosterone Gel Recalled by Teva Pharmaceuticals USA, Inc Due to...

The Issue: Superpotent Drug

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceAugust 8, 2024· Epilog Laser Corp.

Recalled Item: Fusion Pro 24 Recalled by Epilog Laser Corp. Due to a. A small number of...

The Issue: a. A small number of Fusion Pro 24 units were released with an incorrectly...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2024· Alcon Research LLC

Recalled Item: DAILIES TOTAL1 Recalled by Alcon Research LLC Due to Material with a quality...

The Issue: Material with a quality issue was used in contact lens production, so...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2024· GE Healthcare GmbH

Recalled Item: ViewPoint 6 Recalled by GE Healthcare GmbH Due to The National Institute of...

The Issue: The National Institute of Standards and Technology (NIST) has identified in...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2024· B. Braun Medical, Inc.

Recalled Item: AET36 ANESTH EXT SET - Anesthesia Extension Set - Normally Closed Dual...

The Issue: Potential for product leakage from the Spin Lock Connector on the distal end...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2024· GE Healthcare GmbH

Recalled Item: ViewPoint Recalled by GE Healthcare GmbH Due to The National Institute of...

The Issue: The National Institute of Standards and Technology (NIST) has identified in...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2024· Zimmer GmbH

Recalled Item: Biolox Option Taper Sleeve Recalled by Zimmer GmbH Due to Mislabeling

The Issue: Mislabeled: Incorrect sleeve in the packaging. The outer packaging is...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2024· Fresenius Medical Care Holdings, Inc.

Recalled Item: Blood Pressure Module BPM3 TM-2917B (Spare Part Numbers 191378 or Recalled...

The Issue: Machines equipped with BPM3 Blood Pressure Modules (Blood pressure monitor...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2024· Zimmer GmbH

Recalled Item: Biolox Option Taper Sleeve Recalled by Zimmer GmbH Due to Mislabeling

The Issue: Mislabeled: Incorrect sleeve in the packaging. The outer packaging is...

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

Class II — Potential Health HazardOngoing