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. 2,744 recalls have been distributed to South Carolina in the last 12 months.

51,854 total recalls
2,744 in last 12 months

Showing 541560 of 51,854 recalls

Medical DeviceDecember 4, 2025· Merit Medical Systems, Inc.

Recalled Item: Merit Medical Inflation Device.basixCOMPAK.30 atm/bar.20 mL Numbers:...

The Issue: Inflation device handle may detach from the syringe during procedure.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 4, 2025· Merit Medical Systems, Inc.

Recalled Item: Merit Medical Recalled by Merit Medical Systems, Inc. Due to Inflation...

The Issue: Inflation device handle may detach from the syringe during procedure.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 4, 2025· Merit Medical Systems, Inc.

Recalled Item: Merit Medical Recalled by Merit Medical Systems, Inc. Due to Inflation...

The Issue: Inflation device handle may detach from the syringe during procedure.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 4, 2025· Merit Medical Systems, Inc.

Recalled Item: Merit Medical Recalled by Merit Medical Systems, Inc. Due to Inflation...

The Issue: Inflation device handle may detach from the syringe during procedure.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 4, 2025· Merit Medical Systems, Inc.

Recalled Item: Allwell Angioplasty Pack /B Recalled by Merit Medical Systems, Inc. Due to...

The Issue: Inflation device handle may detach from the syringe during procedure.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 4, 2025· Intuitive Surgical, Inc.

Recalled Item: Brand Name: Ion Endoluminal System Product Name: Ion Vision Probe Recalled...

The Issue: Due to probe bags that may have a compromised or incomplete sterile pouch seal.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 4, 2025· Mobius Imaging, LLC

Recalled Item: Detachable 10in Pend FRU-1 Pend component for the AIRO Computed Recalled by...

The Issue: AIRO pendant replacement kits and upgrade do not possess the "Safe Hand...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 4, 2025· Mobius Imaging, LLC

Recalled Item: Detachable 10in Pendant Upgrade component for the AIRO Computed Tomography...

The Issue: AIRO pendant replacement kits and upgrade do not possess the "Safe Hand...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 4, 2025· Medtronic Inc

Recalled Item: Abre Venous Self-Expanding Stent System Recalled by Medtronic Inc Due to...

The Issue: Stents may be impacted by a Nitinol anomaly which causes a reduced stent...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2025· Philips North America

Recalled Item: Ingenia Ambition S. Product Code (REF): 782108. MR systems with Recalled by...

The Issue: The potential for stiffness value errors when viewing exported MR...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2025· Philips North America

Recalled Item: SmartPath to dStream for 3.0T. Product Code (REF): 782145. MR Recalled by...

The Issue: The potential for stiffness value errors when viewing exported MR...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2025· Philips North America

Recalled Item: Evolution Upgrade 1.5T. Product Codes (REF): (1) 782148 Recalled by Philips...

The Issue: The potential for stiffness value errors when viewing exported MR...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2025· Philips North America

Recalled Item: Ingenia 3.0T. Product Code (REF): (1) 781342 Recalled by Philips North...

The Issue: The potential for stiffness value errors when viewing exported MR...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2025· Philips North America

Recalled Item: MR 7700. Product Code (REF): (1) 782120 Recalled by Philips North America...

The Issue: The potential for stiffness value errors when viewing exported MR...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2025· Philips North America

Recalled Item: Ingenia 3.0T CX. Product Code (REF): 781271. MR systems with Recalled by...

The Issue: The potential for stiffness value errors when viewing exported MR...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2025· Philips North America

Recalled Item: Ingenia Elition X. Product Code (REF): (1) 781358 Recalled by Philips North...

The Issue: The potential for stiffness value errors when viewing exported MR...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2025· Philips North America

Recalled Item: Evolution Upgrade 3.0T. Product Code (REF): 782143. MR systems with Recalled...

The Issue: The potential for stiffness value errors when viewing exported MR...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2025· Philips North America

Recalled Item: SmartPath to dStream for XR and 3.0T. Product Code (REF): Recalled by...

The Issue: The potential for stiffness value errors when viewing exported MR...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2025· Philips North America

Recalled Item: Ingenia Ambition X. Product Code (REF): (1) 781356 Recalled by Philips North...

The Issue: The potential for stiffness value errors when viewing exported MR...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2025· Philips North America

Recalled Item: Ingenia Elition S. Product Code (REF): (1) 781357 Recalled by Philips North...

The Issue: The potential for stiffness value errors when viewing exported MR...

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

Class II — Potential Health HazardOngoing