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 2592125940 of 28,688 recalls

Medical DeviceJuly 31, 2013· Synthes USA HQ, Inc.

Recalled Item: Synthes Tensioning Device The Synthes Osteogenesis System Recalled by...

The Issue: All lots of the Synthes Tensioning Device were recalled due to the potential...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 31, 2013· Synthes USA HQ, Inc.

Recalled Item: Synthes Matrix Threaded Persuader Deformity is a comprehensive thoracolumbar...

The Issue: Synthes became aware that during a procedure using the Matrix Threaded...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 31, 2013· Fujinon Inc

Recalled Item: Fujinon/Fujifilm Ultrasonic Endoscope Intended to provide ultrasonic images...

The Issue: A limited number of endoscopes were shipped to FMSU-ESD with a manufacturing...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 31, 2013· Boston Scientific Corporation

Recalled Item: Boston Scientific Recalled by Boston Scientific Corporation Due to Boston...

The Issue: Boston Scientific is initiating a recall removal of the 4.0mm x 15mm size of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 31, 2013· Boston Scientific Corporation

Recalled Item: Boston Scientific Recalled by Boston Scientific Corporation Due to Boston...

The Issue: Boston Scientific is initiating a recall removal of the 4.0mm x 15mm size of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 31, 2013· DePuy Spine, Inc.

Recalled Item: PIPELINE LS ACCESS SYSTEM Recalled by DePuy Spine, Inc. Due to Dilators and...

The Issue: Dilators and Holding Clip are being used for a secondary function of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 31, 2013· DePuy Spine, Inc.

Recalled Item: PIPELINE LS ACCESS SYSTEM Recalled by DePuy Spine, Inc. Due to Dilators and...

The Issue: Dilators and Holding Clip are being used for a secondary function of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 31, 2013· DePuy Spine, Inc.

Recalled Item: PIPELINE LS ACCESS SYSTEM Recalled by DePuy Spine, Inc. Due to Dilators and...

The Issue: Dilators and Holding Clip are being used for a secondary function of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 31, 2013· Synthes USA HQ, Inc.

Recalled Item: Slipped Capital Femoral Epiphysis System Product Usage: Intended for...

The Issue: There is a possibility for the Guide Wires of the Slipped Capital Femoral...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 31, 2013· DePuy Spine, Inc.

Recalled Item: PIPELINE LS ACCESS SYSTEM Recalled by DePuy Spine, Inc. Due to Dilators and...

The Issue: Dilators and Holding Clip are being used for a secondary function of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 31, 2013· Leica Biosystems Newcastle Ltd.

Recalled Item: Leica BIOSYSTEMS Recalled by Leica Biosystems Newcastle Ltd. Due to The...

The Issue: The affected lots of the product may contain a contaminant of fungus that...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 31, 2013· DePuy Spine, Inc.

Recalled Item: PIPELINE LS ACCESS SYSTEM Recalled by DePuy Spine, Inc. Due to Dilators and...

The Issue: Dilators and Holding Clip are being used for a secondary function of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 31, 2013· Synthes USA HQ, Inc.

Recalled Item: 2.4 and 2.7 MM Locking Screw SLF-TPNG with T8 Stardrive Recalled by Synthes...

The Issue: Specific lots of the SS 2.4mm and SS 2.7mm Locking Screw (self-tapping) due...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 31, 2013· Edwards Lifesciences, LLC

Recalled Item: "***Flo Trac Sensor Model MHD85***" Sterile Recalled by Edwards...

The Issue: The Edwards Lifesciences FloTrac Sensor is being recalled due to a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 30, 2013· Stryker Craniomaxillofacial Division

Recalled Item: Stryker Part Numbers 79-43903 (3cc) Recalled by Stryker Craniomaxillofacial...

The Issue: Stryker received reports of the desiccant bag in the kit leaking silica gel...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 30, 2013· Synthes USA HQ, Inc.

Recalled Item: Synthes 2.4 VA-LCP 2 CLMN VLR DSTL Radius PL 7H Recalled by Synthes USA HQ,...

The Issue: The possibility exists that 2.4 mm VA-LCP 2 column distal radius plates from...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 30, 2013· Getinge Disinfection

Recalled Item: Getinge 46-Series Medical Washer-Disinfectors Recalled by Getinge...

The Issue: Getinge Disinfection AB initiated a voluntary field safety correction for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 30, 2013· Synthes USA HQ, Inc.

Recalled Item: Synthes Titanium Cannulated Humeral Nail Intended to aid in the Recalled by...

The Issue: The packaging incorrectly depicts the Synthes Titanium Cannulated Humeral...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 30, 2013· Synthes USA HQ, Inc.

Recalled Item: Titanium Trochanteric Fixation Nail (TFN)System Intended to treat stable and...

The Issue: Two lots of Titanium Trochanteric Fixation Nail (TFN) System are missing the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 30, 2013· Edwards Lifesciences, LLC

Recalled Item: Edwards Lifesciences Anastaflo Intravascular Shunt Recalled by Edwards...

The Issue: Edwards Lifesciences is recalling certain lots of the Anastaflo...

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

Class II — Potential Health HazardOngoing