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. 2,380 recalls have been distributed to North Dakota in the last 12 months.
Showing 23081–23100 of 27,512 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: 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: 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.
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: 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: 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: Zenith Slide W-I-D-E Long Term Care Bed Recalled by GF Health Products,...
The Issue: The bed head deck may fail to elevate as expected during normal operation....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
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.
Recalled Item: RENASYS EZ/ RENASYS EZ Plus 800 mL canister (w/o CLP) Recalled by Smith &...
The Issue: RENASYS EZ Canisters exhibiting visible evidence of deformation of the inlet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RENASYS EZ/ RENASYS EZ Plus 800 mL canister with Solidifier Recalled by...
The Issue: RENASYS EZ Canisters exhibiting visible evidence of deformation of the inlet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stago IVD Recalled by Diagnostica Stago, Inc. Due to Diagnostica Stago Inc....
The Issue: Diagnostica Stago Inc. received some customer complaints regarding a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RENASYS EZ/ RENASYS EZ Plus 250 mL canister with Solidifier Recalled by...
The Issue: RENASYS EZ Canisters exhibiting visible evidence of deformation of the inlet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pedi-Pak Pedi-Syringe Filter 30 mL Becton Dickinson Syringe Rx Only Genesis...
The Issue: Genesis BPS is recalling numerous devices since they did not notify the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pedi-Pak Pedi-Syringe Filter 35 mL Monoject Syringe Rx Only Genesis BPS...
The Issue: Genesis BPS is recalling numerous devices since they did not notify the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TomoTherapy Treatment System Recalled by TomoTherapy Incorporated Due to...
The Issue: Accuray is voluntarily recalling TomoTherapy H Series software versions...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.