Product Recalls in South Carolina

Product recalls affecting South Carolina — including food, drugs, consumer products, medical devices, and vehicles distributed to South Carolina. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,087 recalls have been distributed to South Carolina in the last 12 months.

51,854 total recalls
2,087 in last 12 months

Showing 38413860 of 28,688 recalls

Medical DeviceMay 16, 2024· Inspire Medical Systems Inc.

Recalled Item: Inspire Model 3028 Recalled by Inspire Medical Systems Inc. Due to There is...

The Issue: There is a potential manufacturing defect which can lead to electrical...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 16, 2024· Abbott Medical

Recalled Item: Abbott Liberta RC Recalled by Abbott Medical Due to Deep brain stimulation...

The Issue: Deep brain stimulation system will first turn off after approximately 50...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2024· Medtronic Perfusion Systems

Recalled Item: TourniKwik Tourniquet Set (CFN 79012) Recalled by Medtronic Perfusion...

The Issue: Incorrect component placed in four manufactured lots of the TourniKwik"...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2024· BioFire Diagnostics, LLC

Recalled Item: BIOFIRE FILMARRAY Gastrointestinal (GI) Panel (30 test kit) Recalled by...

The Issue: Due to increase of false positive Vibrio/Vibrio Cholerae results when using...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2024· Abbott Medical

Recalled Item: Abbott Proclaim XR 5 Implantable Pulse Generator Recalled by Abbott Medical...

The Issue: The duration between the implantable pulse generator reaching the elective...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2024· Abbott Medical

Recalled Item: Abbott Proclaim 5 Implantable Pulse Generator Recalled by Abbott Medical Due...

The Issue: The duration between the implantable pulse generator reaching the elective...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2024· Abbott Medical

Recalled Item: Abbott Proclaim 7 Implantable Pulse Generator Recalled by Abbott Medical Due...

The Issue: The duration between the implantable pulse generator reaching the elective...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2024· Abbott Medical

Recalled Item: Abbott Proclaim XR 7 Implantable Pulse Generator Recalled by Abbott Medical...

The Issue: The duration between the implantable pulse generator reaching the elective...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2024· Abbott Medical

Recalled Item: Abbott Proclaim Plus 7 Implantable Pulse Generator Recalled by Abbott...

The Issue: The duration between the implantable pulse generator reaching the elective...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2024· Abbott Medical

Recalled Item: Abbott Proclaim Plus 5 Implantable Pulse Generator Recalled by Abbott...

The Issue: The duration between the implantable pulse generator reaching the elective...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2024· Abbott Medical

Recalled Item: Abbott Proclaim DRG Implantable Pulse Generator Recalled by Abbott Medical...

The Issue: The duration between the implantable pulse generator reaching the elective...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2024· Abbott Medical

Recalled Item: Abbott Proclaim Plus 5 Implantable Pulse Generator Recalled by Abbott...

The Issue: The duration between the implantable pulse generator reaching the elective...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2024· Abbott Medical

Recalled Item: Proclaim 7 Elite Implantable Pulse Generator Recalled by Abbott Medical Due...

The Issue: The duration between the implantable pulse generator reaching the elective...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2024· Abbott Medical

Recalled Item: Abbott Proclaim 7 Implantable Pulse Generator Recalled by Abbott Medical Due...

The Issue: The duration between the implantable pulse generator reaching the elective...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2024· Abbott Medical

Recalled Item: Proclaim 5 Elite Implantable Pulse Generator Recalled by Abbott Medical Due...

The Issue: The duration between the implantable pulse generator reaching the elective...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2024· American Contract Systems Inc

Recalled Item: MAJOR KNEE - 302497- Procedure tray Catalog Number: ASKN23B Recalled by...

The Issue: Ethylene Oxide/Ethylene Chlorohydrin (EO/ECH) residuals for the cast padding...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2024· American Contract Systems Inc

Recalled Item: HAND WRIST FOREARM-LF Procedure tray Catalog Number: CCHD17B Recalled by...

The Issue: Ethylene Oxide/Ethylene Chlorohydrin (EO/ECH) residuals for the cast padding...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2024· American Contract Systems Inc

Recalled Item: ORIF HIP - IM RODDING FEMUR-Procedure Kit Catalog Number: UTHP44S Recalled...

The Issue: Ethylene Oxide/Ethylene Chlorohydrin (EO/ECH) residuals for the cast padding...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2024· American Contract Systems Inc

Recalled Item: CUSTOM KNEE - 206061-Procedure Kit Catalog Number: UDKN68AE Recalled by...

The Issue: Ethylene Oxide/Ethylene Chlorohydrin (EO/ECH) residuals for the cast padding...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2024· American Contract Systems Inc

Recalled Item: TOTAL KNEE - 297835-Procedure Kit Catalog Number: RGTK10K Recalled by...

The Issue: Ethylene Oxide/Ethylene Chlorohydrin (EO/ECH) residuals for the cast padding...

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

Class II — Potential Health HazardOngoing