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. 2,743 recalls have been distributed to South Carolina in the last 12 months.

51,854 total recalls
2,743 in last 12 months

Showing 19011920 of 28,688 recalls

Medical DeviceMarch 19, 2025· Avanos Medical, Inc.

Recalled Item: Brand Name: Ballard Product Name: Closed Suction Catheters Model/Catalog...

The Issue: Lack of sterility assurance for closed suction catheter systems

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 19, 2025· Avanos Medical, Inc.

Recalled Item: Brand Name: Ballard Product Name: Closed Suction Catheters Model/Catalog...

The Issue: Lack of sterility assurance for closed suction catheter systems

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 18, 2025· Smith & Nephew, Inc.

Recalled Item: META-TAN LAG/COMPRESSION SCREW KIT 90MM/85MM Recalled by Smith & Nephew,...

The Issue: Integrated Lag/Compression Screw Kit has a compression screw with hexagon...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 18, 2025· Abbott Laboratories

Recalled Item: Brand Name: CELL-DYN Ruby Product Name: CELL-DYN Ruby Model/Catalog Number:...

The Issue: When expired reagents are scanned or manually entered, the system will...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 18, 2025· Abbott Laboratories

Recalled Item: Brand Name: CELL-DYN Ruby Product Name: CELL-DYN Ruby Model/Catalog Number:...

The Issue: When expired reagents are scanned or manually entered, the system will...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 18, 2025· Abbott Laboratories

Recalled Item: Brand Name: CELL-DYN Ruby Product Name: CELL-DYN Ruby Model/Catalog Number:...

The Issue: When expired reagents are scanned or manually entered, the system will...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 18, 2025· Abbott Laboratories

Recalled Item: Brand Name: CELL-DYN Ruby Product Name: CELL-DYN Ruby Model/Catalog Number:...

The Issue: When expired reagents are scanned or manually entered, the system will...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 18, 2025· Abbott Laboratories

Recalled Item: Brand Name: CELL-DYN Ruby Product Name: CELL-DYN Ruby Model/Catalog Number:...

The Issue: When expired reagents are scanned or manually entered, the system will...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2025· Beckman Coulter Inc.

Recalled Item: DxC 500 AU Clinical Chemistry Analyzer Recalled by Beckman Coulter Inc. Due...

The Issue: The reason for the recall is incorrect sample barcode identification and...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2025· Abbott

Recalled Item: Amplatzer TorqVue LP Delivery System (TVLP) Recalled by Abbott Due to Device...

The Issue: Device may have a small breach in the proximal end of the shaft under the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2025· Abbott

Recalled Item: Amplatzer TorqVue LP Catheter (TVLPC) Recalled by Abbott Due to Device may...

The Issue: Device may have a small breach in the proximal end of the shaft under the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 14, 2025· ESAOTE S.P.A.

Recalled Item: Esaote Endocavity ultrasonic probe Recalled by ESAOTE S.P.A. Due to A...

The Issue: A potential weakness has been identified in the probe body, so that, in a...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 14, 2025· Pro-Med Instruments Gmbh

Recalled Item: DORO¿ Easy-Connect Navigation Adaptor Recalled by Pro-Med Instruments Gmbh...

The Issue: Potential of compromised compatibility resulting in influence on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 14, 2025· Merit Medical Systems, Inc.

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

The Issue: Update to IFU to provide additional information related to risk with device...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 14, 2025· Merit Medical Systems, Inc.

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

The Issue: Update to IFU to provide additional information related to risk with device...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 13, 2025· Thoratec LLC

Recalled Item: HeartMate Mobile Power Unit: Recalled by Thoratec LLC Due to Left...

The Issue: Left Ventricular Assist System Mobile Power Unit (MPU) may have electrical...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 12, 2025· Draeger, Inc.

Recalled Item: Brand Name: VentStar Product Name: VentStar Flex 220 Model/Catalog Number:...

The Issue: The potential for cracks forming in the breathing circuit hose.

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 12, 2025· Draeger, Inc.

Recalled Item: Brand Name: Anesthesia Circuit Kit Product Name: Anesthesia Circuit Kit...

The Issue: The potential for cracks forming in the breathing circuit hose.

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 12, 2025· Draeger, Inc.

Recalled Item: Brand Name: Anesthesia Circuit Kit Product Name: Anesthesia Circuit Kit...

The Issue: The potential for cracks forming in the breathing circuit hose.

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 12, 2025· Draeger, Inc.

Recalled Item: Brand Name: Anesthesia Circuit Kit Product Name: Anesthesia Circuit Kit...

The Issue: The potential for cracks forming in the breathing circuit hose.

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

Class I — Serious Health HazardOngoing