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. 2,699 recalls have been distributed to South Carolina in the last 12 months.

51,854 total recalls
2,699 in last 12 months

Showing 1064110660 of 28,688 recalls

Medical DeviceNovember 23, 2020· Fresenius Medical Care Holdings, Inc.

Recalled Item: Naturalyte Liquid Acid concentrate drums Recalled by Fresenius Medical Care...

The Issue: The deviation in conductivity for sodium level exceeds 0.6mS/cm from the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 23, 2020· Fresenius Medical Care Holdings, Inc.

Recalled Item: Naturalyte Liquid Acid concentrate bottles Recalled by Fresenius Medical...

The Issue: The deviation in conductivity for sodium level exceeds 0.6mS/cm from the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 23, 2020· Covidien Llc

Recalled Item: Covidien TA Auto Suture Vascular Loading Unit with DST Series Recalled by...

The Issue: May contain a damaged internal component which could impede staple...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 23, 2020· Covidien Llc

Recalled Item: Covidien TA Auto Suture Vascular Stapler with DST Series Technology Recalled...

The Issue: May contain a damaged internal component which could impede staple...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 23, 2020· GE Healthcare, LLC

Recalled Item: Revolution CT ES - Product Usage: intended for head Recalled by GE...

The Issue: A potential for protocol(s) with unintended patient orientation or scan...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 23, 2020· B Braun Medical, Inc.

Recalled Item: APEX Compounding System Control Panel Module Recalled by B Braun Medical,...

The Issue: There is the potential for the compounding system to not immediately...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 23, 2020· GE Healthcare, LLC

Recalled Item: Revolution CT with Apex Edition CT System - Product Usage: intended for head...

The Issue: A potential for protocol(s) with unintended patient orientation or scan...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 23, 2020· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Atellica Gamma-Glutamyl Transferase (GGT) Reagent - Product Usage: For in...

The Issue: Gamma-Glutamyl Transferase (GGT) Reagent Low End Repeatability-Imprecision....

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 23, 2020· Siemens Healthcare Diagnostics, Inc.

Recalled Item: ADVIA Gamma-Glutamyl Transferase (GGT) Reagent - Product Usage: For in...

The Issue: Gamma-Glutamyl Transferase (GGT) Reagent Low End Repeatability-Imprecision....

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 23, 2020· B Braun Medical, Inc.

Recalled Item: APEX Compounding System Control Panel Module Recalled by B Braun Medical,...

The Issue: There is the potential for the compounding system to not immediately...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 23, 2020· Baxter Healthcare Corporation

Recalled Item: Baxter SIGMA Spectrum Infusion Pump with Master Drug Library (Version...

The Issue: There is a potential software error during programming.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 23, 2020· Baxter Healthcare Corporation

Recalled Item: Baxter Spectrum IQ Infusion System with Dose IQ Safety Software Recalled by...

The Issue: There is a potential software error during programming.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 23, 2020· Baxter Healthcare Corporation

Recalled Item: Baxter SIGMA Spectrum Infusion Pump with Master Drug Library (Version...

The Issue: There is a potential software error during programming.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 23, 2020· B Braun Medical, Inc.

Recalled Item: APEX Compounding System Control Panel Module Recalled by B Braun Medical,...

The Issue: There is the potential for the compounding system to not immediately...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 23, 2020· Baxter Healthcare Corporation

Recalled Item: Baxter SIGMA Spectrum Infusion Pump with Master Drug Library (Version...

The Issue: There is a potential software error during programming.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 20, 2020· Ortho-Clinical Diagnostics, Inc.

Recalled Item: enGen Laboratory Automation System Recalled by Ortho-Clinical Diagnostics,...

The Issue: A software anomaly may cause an aliquoted sample to be labelled as the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 20, 2020· Ortho-Clinical Diagnostics, Inc.

Recalled Item: VITROS Automation Solutions Recalled by Ortho-Clinical Diagnostics, Inc. Due...

The Issue: A software anomaly may cause an aliquoted sample to be labelled as the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 20, 2020· Zimmer Biomet, Inc.

Recalled Item: Spinal Rod Cutter Recalled by Zimmer Biomet, Inc. Due to Device has the...

The Issue: Device has the potential for fracture during use.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 20, 2020· Haag-Streit USA Inc

Recalled Item: Haag Streit Surgical Floor stands FS 2-11 (. 615H511) Recalled by...

The Issue: Software error -Software 588 versions 2.0 to 3.3, movement of the focusing...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 20, 2020· Maquet Cardiovascular Us Sales, Llc

Recalled Item: HLS Set Advanced Model Name: BEQ-HLS 5050 USA Recalled by Maquet...

The Issue: The HLS Set Advanced (disposable for Cardiohelp) is being recalled due to...

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

Class II — Potential Health HazardOngoing