Product Recalls in North Carolina
Product recalls affecting North Carolina — including food, drugs, consumer products, medical devices, and vehicles distributed to North Carolina. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,932 recalls have been distributed to North Carolina in the last 12 months.
Showing 18681–18700 of 29,737 recalls
Recalled Item: TIBIAL I/M NAIL 15MMDX26CM Recalled by Zimmer Biomet, Inc. Due to Zimmer...
The Issue: Zimmer Biomet is initiating a field action for sterile-packaged implants...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FEM IM NAIL 14MMDX30CM LEFT Recalled by Zimmer Biomet, Inc. Due to Zimmer...
The Issue: Zimmer Biomet is initiating a field action for sterile-packaged implants...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Z NAIL PF 14MM X 46CM UNIV Z NAIL GT Recalled by Zimmer Biomet, Inc. Due to...
The Issue: Zimmer Biomet is initiating a field action for sterile-packaged implants...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1000 ml Canister (with Gel) for InfoV.A.C. and V.A.C.ULTA Therapy Recalled...
The Issue: Potential sterile barrier breach
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VERSA-FXII SC TUBE PLT 90DX16H Recalled by Zimmer Biomet, Inc. Due to Zimmer...
The Issue: Zimmer Biomet is initiating a field action for sterile-packaged implants...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow(R) VPS(R) Access Kit for use with 4 and 5 Recalled by Arrow...
The Issue: Arrow International is notifying each customer who received the affected...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TI Transport Monitor/Module Battery Pack Product Usage: intended for...
The Issue: Mindray has received two reports from outside the United States that the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AbbVie PEG Recalled by AbbVie Inc. Due to
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AbbVie PEG Recalled by AbbVie Inc. Due to PEG kits have the potential for...
The Issue: PEG kits have the potential for one of the following defects: missing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AbbVie PEG Recalled by AbbVie Inc. Due to PEG kits have the potential for...
The Issue: PEG kits have the potential for one of the following defects: missing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AirLife Resuscitation Recalled by Vyaire Medical Due to The mask component...
The Issue: The mask component on various lots of the resuscitation devices have been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AirLife Resuscitation Recalled by Vyaire Medical Due to The mask component...
The Issue: The mask component on various lots of the resuscitation devices have been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AirLife Resuscitation Recalled by Vyaire Medical Due to The mask component...
The Issue: The mask component on various lots of the resuscitation devices have been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AirLife Resuscitation Recalled by Vyaire Medical Due to The mask component...
The Issue: The mask component on various lots of the resuscitation devices have been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AirLife Resuscitation Recalled by Vyaire Medical Due to The mask component...
The Issue: The mask component on various lots of the resuscitation devices have been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AirLife Resuscitation Recalled by Vyaire Medical Due to The mask component...
The Issue: The mask component on various lots of the resuscitation devices have been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AirLife Resuscitation Recalled by Vyaire Medical Due to The mask component...
The Issue: The mask component on various lots of the resuscitation devices have been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AirLife Resuscitation Recalled by Vyaire Medical Due to The mask component...
The Issue: The mask component on various lots of the resuscitation devices have been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AirLife Resuscitation Recalled by Vyaire Medical Due to The mask component...
The Issue: The mask component on various lots of the resuscitation devices have been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AirLife Resuscitation Recalled by Vyaire Medical Due to The mask component...
The Issue: The mask component on various lots of the resuscitation devices have been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.