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. 2,529 recalls have been distributed to South Carolina in the last 12 months.

51,854 total recalls
2,529 in last 12 months

Showing 2560125620 of 28,688 recalls

Medical DeviceOctober 11, 2013· Zimmer, Inc.

Recalled Item: 6 DEGREE COCR FEM HEAD (various sizes) and 6 DEG UNIPOLAR FEMORAL HE...

The Issue: Zimmer recently conducted a review of all historic packaging validations at...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 11, 2013· Zimmer, Inc.

Recalled Item: ITST ANTI-ROTATION SCREW and FEM IM NAIL (10MM Recalled by Zimmer, Inc. Due...

The Issue: Zimmer recently conducted a review of all historic packaging validations at...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 11, 2013· Zimmer, Inc.

Recalled Item: MODULAR AUSTIN MOORE SOLI and MOORE HIP PROS REG SOLID Recalled by Zimmer,...

The Issue: Zimmer recently conducted a review of all historic packaging validations at...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 10, 2013· Biomet, Inc.

Recalled Item: Juggerknotless Drill Bit Recalled by Biomet, Inc. Due to Investigation...

The Issue: Investigation identified that the design of the drill bit may make the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 10, 2013· Mizuho America, Inc.

Recalled Item: Mizuho Sugita Titanium Standard Aneurysm Clip II Recalled by Mizuho America,...

The Issue: Specific item numbers form Lots 27-J and 29-J of Sugita T2 Aneurysm Clips....

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 10, 2013· Mizuho America, Inc.

Recalled Item: Mizuho Sugita Titanium Standard Aneurysm Clip II Recalled by Mizuho America,...

The Issue: Specific item numbers form Lots 27-J and 29-J of Sugita T2 Aneurysm Clips....

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 10, 2013· Ortho-Clinical Diagnostics

Recalled Item: VITROS Chemistry Products Mixing Cup Arrays utilized on VITROS 250 Recalled...

The Issue: Ortho Clinical Diagnostics issued a product correction notification for...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 10, 2013· Nova Biomedical Corporation

Recalled Item: Nova StatStrip/StatSensor Hospital Blood Glucose Meter Recalled by Nova...

The Issue: Revised Battery Instructions for Removal and Expiration Date due to battery...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 10, 2013· Cayenne Medical Inc.

Recalled Item: Drill (Fluted-Hard Bone) Recalled by Cayenne Medical Inc. Due to A review of...

The Issue: A review of complaints identified a trend for drills breaking.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 10, 2013· Stryker Howmedica Osteonics Corp.

Recalled Item: VariAx Compression Plating System Recalled by Stryker Howmedica Osteonics...

The Issue: Stryker received two reports indicating that during screw insertion under a...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 9, 2013· Neurotherm, Inc.

Recalled Item: Neurotherm NT2000iX RF Generator Model Number: RFG-NT -2000iX Recalled by...

The Issue: NT2000iX software shipped with the international setting turned on. The...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 9, 2013· Zimmer, Inc.

Recalled Item: Trinica Anterior Lumbar Plate (ALP) system Recalled by Zimmer, Inc. Due to...

The Issue: Zimmer Spine, Inc. is initiating a correction regarding the Trinica ALP...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 9, 2013· GE Healthcare, LLC

Recalled Item: GE Optima CT520 and Optima CT540 Computed Tomography (CT) systems. Recalled...

The Issue: There is an issue with the Manual Film Composer feature on some CT products....

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 9, 2013· Arrow International Inc

Recalled Item: Arrow Transradial Artery Access products Arrow Transradial Artery Access...

The Issue: There is a risk that the introducer needles packaged within the kits can be...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 9, 2013· Arrow International Inc

Recalled Item: Continuous Peripheral Nerve Block Catheter Kit and Set Continuous Peripheral...

The Issue: A labeling inconsistency was discovered in which the lidstock states that...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 9, 2013· Synthes USA HQ, Inc.

Recalled Item: Synthes TomoFix Plates The Synthes J5606-C TomoFix Osteotomy System is...

The Issue: A labeling correction was initiated related to the Surgical Technique Guide...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 9, 2013· Ortho-Clinical Diagnostics

Recalled Item: VITROS CA 125 II Calibrators For use in the calibration Recalled by...

The Issue: Ortho Clinical Diagnostics issued a Product Correction Notification for...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 8, 2013· Synthes USA HQ, Inc.

Recalled Item: Synthes Implant Holder for Synfix (TM)-LR the Synthes Implant Holder...

The Issue: Complaints were received which described the SynFix LR implant holder...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 8, 2013· Ortho-Clinical Diagnostics

Recalled Item: enGen Track System with enGen Select v5.0 with autoverification enabled...

The Issue: Ortho Clinical Diagnostics issued an Urgent Product Correction Notification...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 8, 2013· Ortho-Clinical Diagnostics

Recalled Item: enGen Track System with enGen Custom v3.2.2 (& below) Product The VITROS 5...

The Issue: Ortho Clinical Diagnostics issued an Urgent Product Correction Notification...

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

Class II — Potential Health HazardOngoing