Product Recalls in Mississippi
Product recalls affecting Mississippi — including food, drugs, consumer products, medical devices, and vehicles distributed to Mississippi. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,553 recalls have been distributed to Mississippi in the last 12 months.
Showing 17801–17820 of 28,172 recalls
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: 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: 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: 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: R-F IM NAIL 10MMDX48CM LG 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 15MMDX30CM Recalled by Zimmer Biomet, Inc. Due to Zimmer Biomet...
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: VERSA-FX II STD TUBE 130DX16H 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: 4.5 BROAD SCP PLT 26-H STER 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: 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
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.