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. 2,672 recalls have been distributed to South Carolina in the last 12 months.

51,854 total recalls
2,672 in last 12 months

Showing 1176111780 of 28,688 recalls

Medical DeviceMay 14, 2020· Biomet

Recalled Item: A.L.P.S. PROXIMAL HUMERUS PLATING SYSTEM LOW PLATE RIGHT 14 HOLE 227MM...

The Issue: Distributed to the field without having completed design history files or...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 14, 2020· Biomet

Recalled Item: A.L.P.S. PROXIMAL HUMERUS PLATING SYSTEM HIGH PLATE RIGHT 7 HOLE 140MM...

The Issue: Distributed to the field without having completed design history files or...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 14, 2020· Biomet

Recalled Item: A.L.P.S.¿ PROXIMAL HUMERUS PLATING SYSTEM LOW PLATE LEFT 14 HOLE 227MM...

The Issue: Distributed to the field without having completed design history files or...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 14, 2020· Biomet

Recalled Item: Biomet 6.5 Cannulated Screw Tap - Bone fixation screw Recalled by Biomet Due...

The Issue: Distributed to the field without having completed design history files or...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 12, 2020· DiaSorin Molecular LLC

Recalled Item: MOL3655 Simplexa VZV Swab Direct - Product Usage: is intended Recalled by...

The Issue: Due to a software malfunction in the Multi Assay Suite, there is the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 12, 2020· DiaSorin Molecular LLC

Recalled Item: MOL2150 Simplexa HSV 1&2 Direct -CSF -Genital Swab -Cutaneous / Recalled by...

The Issue: Due to a software malfunction in the Multi Assay Suite, there is the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 12, 2020· DiaSorin Molecular LLC

Recalled Item: MOL3650 Simplexa VZV Direct - Product Usage: is intended for Recalled by...

The Issue: Due to a software malfunction in the Multi Assay Suite, there is the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 12, 2020· Abbott Gmbh & Co. KG

Recalled Item: Alinity C Recalled by Abbott Gmbh & Co. KG Due to There is a potential to...

The Issue: There is a potential to generate incorrect patient results for the following...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 12, 2020· Med Tec Inc

Recalled Item: Type S Extension For use with Varian Recalled by Med Tec Inc Due to...

The Issue: Potential for disengagement of the Varian Style Type-S Extension during...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 11, 2020· Radiometer Medical ApS

Recalled Item: ABL80-FLEX CO-OX 393-841 Box Label Recalled by Radiometer Medical ApS Due to...

The Issue: Barcode readers on ALB900 and ABL800 analyzers used for measuring pH, blood...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 11, 2020· Radiometer Medical ApS

Recalled Item: ABL80-FLEX-393-839 Box Label Recalled by Radiometer Medical ApS Due to...

The Issue: Barcode readers on ALB900 and ABL800 analyzers used for measuring pH, blood...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 11, 2020· Ortho-Clinical Diagnostics

Recalled Item: VITROS Chemistry Product Performance Verifier I Recalled by Ortho-Clinical...

The Issue: Multiple coatings of VITROS Chemistry Products AMYL Slides are showing...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 11, 2020· Ortho-Clinical Diagnostics

Recalled Item: VITROS Chemistry Product AMYL Slides Reagent Recalled by Ortho-Clinical...

The Issue: Multiple coatings of VITROS Chemistry Products AMYL Slides are showing...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 11, 2020· Ortho-Clinical Diagnostics

Recalled Item: VITROS Chemistry Product Performance Verifier II Recalled by Ortho-Clinical...

The Issue: Multiple coatings of VITROS Chemistry Products AMYL Slides are showing...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 11, 2020· Ortho-Clinical Diagnostics

Recalled Item: VITROS Chemistry Product AMYL Slides Reagent Recalled by Ortho-Clinical...

The Issue: Multiple coatings of VITROS Chemistry Products AMYL Slides are showing...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 11, 2020· Biomet, Inc.

Recalled Item: Comprehensive VRS Inserter Recalled by Biomet, Inc. Due to The product is...

The Issue: The product is being recalled due to the central screw drill seizing inside...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 8, 2020· Ge Healthcare

Recalled Item: The OEC 9900 C-Arm is designed to provide fluoroscopic and Recalled by Ge...

The Issue: GEHC Surgery became aware that some users of the 9800 and 9900 fluoroscopic...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 8, 2020· Merge Healthcare, Inc.

Recalled Item: Merge Healthcare Merge Application Server Software Release and Merge...

The Issue: An error in the calculation of the Michigan Ranges can generate an...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 7, 2020· Stryker GmbH

Recalled Item: Stryker Compression Screw Recalled by Stryker GmbH Due to Seal integrity of...

The Issue: Seal integrity of the blister pack may be compromised and sterility cannot...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 7, 2020· Stryker GmbH

Recalled Item: Stryker Locking Screw Recalled by Stryker GmbH Due to Seal integrity of the...

The Issue: Seal integrity of the blister pack may be compromised and sterility cannot...

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

Class II — Potential Health HazardOngoing