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. 2,486 recalls have been distributed to Washington in the last 12 months.

51,768 total recalls
2,486 in last 12 months

Showing 4344143460 of 51,768 recalls

Medical DeviceJuly 23, 2014· Zimmer, Inc.

Recalled Item: 23.5 Deg Rasp Handle Assy- RIGHT Nonsterile Recalled by Zimmer, Inc. Due to...

The Issue: The firm received complaints for failure of the handle to remain assembled...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 23, 2014· Zimmer, Inc.

Recalled Item: VI DBL OFFST W/ LRG STPL Recalled by Zimmer, Inc. Due to The firm received...

The Issue: The firm received complaints for failure of the handle to remain assembled...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 23, 2014· Zimmer, Inc.

Recalled Item: Double Offset Rasp Handle Recalled by Zimmer, Inc. Due to The firm received...

The Issue: The firm received complaints for failure of the handle to remain assembled...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 23, 2014· Zimmer, Inc.

Recalled Item: VER2 DBL OFFSET RASP HANDLE Recalled by Zimmer, Inc. Due to The firm...

The Issue: The firm received complaints for failure of the handle to remain assembled...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 23, 2014· Zimmer, Inc.

Recalled Item: Double Offset Rasp Handle Recalled by Zimmer, Inc. Due to The firm received...

The Issue: The firm received complaints for failure of the handle to remain assembled...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 23, 2014· Zimmer, Inc.

Recalled Item: Double Offset Rasp Handle Recalled by Zimmer, Inc. Due to The firm received...

The Issue: The firm received complaints for failure of the handle to remain assembled...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 23, 2014· Zimmer, Inc.

Recalled Item: 23.5 Deg Rasp Handle Assy- LEFT Nonsterile Recalled by Zimmer, Inc. Due to...

The Issue: The firm received complaints for failure of the handle to remain assembled...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 23, 2014· Zimmer, Inc.

Recalled Item: VER2 HANDLE Recalled by Zimmer, Inc. Due to The firm received complaints for...

The Issue: The firm received complaints for failure of the handle to remain assembled...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 23, 2014· Zimmer, Inc.

Recalled Item: VER2 HANDLE Recalled by Zimmer, Inc. Due to The firm received complaints for...

The Issue: The firm received complaints for failure of the handle to remain assembled...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 23, 2014· Zimmer, Inc.

Recalled Item: Double Offset Rasp Handle Recalled by Zimmer, Inc. Due to The firm received...

The Issue: The firm received complaints for failure of the handle to remain assembled...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 23, 2014· Zimmer, Inc.

Recalled Item: VER2 D8L OFFSET RASP HANDLE Recalled by Zimmer, Inc. Due to The firm...

The Issue: The firm received complaints for failure of the handle to remain assembled...

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

Class II — Potential Health HazardOngoing
FoodJuly 22, 2014· Dancing Star LLC

Recalled Item: Carob Supergreens Chunks of Energy (10# ) Recalled by Dancing Star LLC Due...

The Issue: Product may be contaminated with Salmonella.

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

Class I — Serious Health HazardOngoing
Refund
FoodJuly 22, 2014· Dancing Star LLC

Recalled Item: Date Flax with Turmeric Chunks of Energy (10# ) Recalled by Dancing Star LLC...

The Issue: Product may be contaminated with Salmonella.

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

Class I — Serious Health HazardOngoing
Refund
FoodJuly 22, 2014· Dancing Star LLC

Recalled Item: Bulk organic Carob powder (10# ) Recalled by Dancing Star LLC Due to...

The Issue: Product may be contaminated with Salmonella.

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

Class I — Serious Health HazardOngoing
Refund
FoodJuly 22, 2014· River Canyon Retreat

Recalled Item: Organic Carob Powder Recalled by River Canyon Retreat Due to Potential...

The Issue: Firm was notified by supplier of recall or Organic Carob Powder that they...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJuly 22, 2014· Abbott Laboratories

Recalled Item: ICT Serum Calibrator . For use in the calibration Recalled by Abbott...

The Issue: ICT Serum Calibrator may generate lower than expected Potassium Quality...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 22, 2014· Becton Dickinson & Company

Recalled Item: BD PosiFlush SF Saline Flush Syringe 0.9 Sodium Chloride Injection Recalled...

The Issue: BD received some reports of open seals found on the BD Posiflush SF Flush...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 22, 2014· Zimmer, Inc.

Recalled Item: 4.5 mm Malleolar Screw Sterile zimmer Recalled by Zimmer, Inc. Due to Zimmer...

The Issue: Zimmer is recalling various trauma screws that failed a leak test due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 22, 2014· Zimmer, Inc.

Recalled Item: 6.5 mm Cancellous Screw Fully Threaded Sterile zimmer Recalled by Zimmer,...

The Issue: Zimmer is recalling various trauma screws that failed a leak test due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 22, 2014· Zimmer, Inc.

Recalled Item: 6.5 mm Cancellous Screw 32 mm Thread Length Sterile zimmer Recalled by...

The Issue: Zimmer is recalling various trauma screws that failed a leak test due to...

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

Class II — Potential Health HazardOngoing