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 2598126000 of 28,688 recalls

Medical DeviceJuly 24, 2013· OrthoPediatrics Corp

Recalled Item: 3.2mm Drill Bit. This is a component within the PediLoc Recalled by...

The Issue: OrthoPediatrics has initiated a voluntary recall of Part # 01-1050-002,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 24, 2013· Gyrus Medical, Inc

Recalled Item: GYRUS ACMI Recalled by Gyrus Medical, Inc Due to On April 29, 2013 Olympus...

The Issue: On April 29, 2013 Olympus Surgical Technologies America R&D received results...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 23, 2013· Elekta, Inc.

Recalled Item: Stereotactic Circular Collimator - 3D Line stereotatic Hardware Accessories...

The Issue: Potential for clinical errors.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 22, 2013· Biomet 3i, LLC

Recalled Item: Contra-Angle Torque Driver Kit For Certain Internal Connection Product...

The Issue: During recent revised sterilization validation testing, the included...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 22, 2013· MCKESSON TECHNOLOGIES INC

Recalled Item: Mc Kesson Anesthesia-Rx Model Number 8.0.2 & 8.0.1 with RapiDispense...

The Issue: The firm issued a clinical alert after users reported an issue where the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 22, 2013· Biomet 3i, LLC

Recalled Item: Contra-Angle Torque Driver Kit For Certain and External Connection Product...

The Issue: During recent revised sterilization validation testing, the included...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 22, 2013· Biomet 3i, LLC

Recalled Item: Navigator Surgical Kit Product Usage: Molded plastic tray used in Recalled...

The Issue: During recent revised sterilization validation testing, the included...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 22, 2013· Synthes USA HQ, Inc.

Recalled Item: 3.7mm and 5.0mm Dynamic Locking Screw (DLS) Product Usage: 3.7mm Recalled by...

The Issue: All lots of 3.7mm and 5.0mm Dynamic Locking Screw (DLS) were recalled due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 22, 2013· Biomet 3i, LLC

Recalled Item: Tapered Navigator Certain Surgical Kit Product Usage: Molded plastic tray...

The Issue: During recent revised sterilization validation testing, the included...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 22, 2013· Biomet 3i, LLC

Recalled Item: Contra-Angle Torque Driver Kit Product Usage: Molded plastic tray used...

The Issue: During recent revised sterilization validation testing, the included...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 19, 2013· Instrumentation Laboratory Co.

Recalled Item: ACL TOP 500 CTS Recalled by Instrumentation Laboratory Co. Due to Potential...

The Issue: Potential carryover issue that can can cause shortened APTT clotting times...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 19, 2013· Instrumentation Laboratory Co.

Recalled Item: ACL TOP 300 and ACL TOP 300 CTS (Japan) Recalled by Instrumentation...

The Issue: Potential carryover issue that can can cause shortened APTT clotting times...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 19, 2013· Instrumentation Laboratory Co.

Recalled Item: ACL TOP 700 LAS Recalled by Instrumentation Laboratory Co. Due to Potential...

The Issue: Potential carryover issue that can can cause shortened APTT clotting times...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 19, 2013· Atrium Medical Corporation

Recalled Item: C-QUR Edge Mesh (All sizes and shapes). Intended for use Recalled by Atrium...

The Issue: Additional Instructions for Use and Storage Conditions as Coated mesh can...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 19, 2013· Instrumentation Laboratory Co.

Recalled Item: ACL TOP CTS Recalled by Instrumentation Laboratory Co. Due to Potential...

The Issue: Potential carryover issue that can can cause shortened APTT clotting times...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 19, 2013· Blue Belt Technologies MN

Recalled Item: Blue Belt Technologies Recalled by Blue Belt Technologies MN Due to Blue...

The Issue: Blue Belt Technologies is recalling sterile Monitor Drapes used with their...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 19, 2013· Instrumentation Laboratory Co.

Recalled Item: ACL TOP (Base) Recalled by Instrumentation Laboratory Co. Due to Potential...

The Issue: Potential carryover issue that can can cause shortened APTT clotting times...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 19, 2013· Atrium Medical Corporation

Recalled Item: C-QUR TacShield Mesh (All sizes and shapes). Intended for use Recalled by...

The Issue: Additional Instructions for Use and Storage Conditions as Coated mesh can...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 19, 2013· Atrium Medical Corporation

Recalled Item: C-QUR Mesh (All Sizes Recalled by Atrium Medical Corporation Due to...

The Issue: Additional Instructions for Use and Storage Conditions as Coated mesh can...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 19, 2013· Instrumentation Laboratory Co.

Recalled Item: ACL TOP 700 Recalled by Instrumentation Laboratory Co. Due to Potential...

The Issue: Potential carryover issue that can can cause shortened APTT clotting times...

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

Class II — Potential Health HazardOngoing