Product Recalls in North Dakota
Product recalls affecting North Dakota — including food, drugs, consumer products, medical devices, and vehicles distributed to North Dakota. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 929 recalls have been distributed to North Dakota in the last 12 months.
Showing 40141–40160 of 47,938 recalls
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
Recalled Item: Vl DBL OFFST WI 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.
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.
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.
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.
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.
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.
Recalled Item: Medtronic MiniMed Guardian Monitor Recalled by Medtronic MiniMed Inc. Due to...
The Issue: Medtronic MiniMed is recalling the Guardian REAL-Time monitors because of a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.