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 2604126060 of 28,688 recalls

Medical DeviceJuly 12, 2013· Atrium Medical Corporation

Recalled Item: Advanta SuperSoft Grafts <6mm Intended for use in arterial vascular Recalled...

The Issue: Inner tray label may adhere to wall of outer tray which make it difficult to...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2013· Atrium Medical Corporation

Recalled Item: Flixene IFG Vascular Grafts >or= 6mm Intended for use in Recalled by Atrium...

The Issue: Inner tray label may adhere to wall of outer tray which make it difficult to...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2013· Atrium Medical Corporation

Recalled Item: Flixene IFG with Assisted Delivery Intended for use in arterial Recalled by...

The Issue: Inner tray label may adhere to wall of outer tray which make it difficult to...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2013· Ormco/Sybronendo

Recalled Item: Brand Name: Vector TAS 8mm Screw. The Device Listing Number Recalled by...

The Issue: Ormco Corporation is voluntarily recalling one lot of 8 MM Vector TAS Screws...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2013· Atrium Medical Corporation

Recalled Item: Advanta VS Grafts <6mm Intended for use in arterial vascular reconstruction...

The Issue: Inner tray label may adhere to wall of outer tray which make it difficult to...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2013· Atrium Medical Corporation

Recalled Item: Advanta SST Grafts <6mm Intended for use in arterial vascular reconstruction...

The Issue: Inner tray label may adhere to wall of outer tray which make it difficult to...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2013· Atrium Medical Corporation

Recalled Item: Advanta SST Grafts >or= 6mm Intended for use in arterial Recalled by Atrium...

The Issue: Inner tray label may adhere to wall of outer tray which make it difficult to...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 11, 2013· Cayenne Medical Inc.

Recalled Item: AperFix AM Femoral Implant Recalled by Cayenne Medical Inc. Due to Potential...

The Issue: Potential for AperFix 24 mm implant breaking inside the drilled femoral socket.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 10, 2013· Smiths Medical ASD, Inc.

Recalled Item: Jelco Smiths Medical Hypodermic Needle-Pro¿ Fixed Needle Insulin Syringe...

The Issue: Visible orange/ brown particulate on the needles of the 29g Hypodermic...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 10, 2013· Precision Dynamics Corporation

Recalled Item: Non-sterile Viscot Surgical Skin Markers Part Number 1437-100 Non-sterile...

The Issue: PDC Healthcare initiated this recall of Non-Sterile Viscot Part Number...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 10, 2013· Siemens Medical Solutions USA, Inc.

Recalled Item: Acuson SC2000 volume imaging ultrasound systems at software version 3.0....

The Issue: Software issue results in inaccurate 3D image may result in ablation in...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 10, 2013· Medical Indicators, Inc.

Recalled Item: Tempa DOT Single-Use Clinical Thermometer Medical Indicators Made in U.S.A....

The Issue: TempaDot products may have been mislabeled.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 10, 2013· Smiths Medical ASD, Inc.

Recalled Item: Jelco Smiths Medical Hypodermic Needle-Pro¿ Fixed Needle Insulin Syringe...

The Issue: Visible orange/ brown particulate on the needles of the 29g Hypodermic...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 10, 2013· Smiths Medical ASD, Inc.

Recalled Item: Jelco Smiths Medical Hypodermic Needle-Pro¿ Fixed Needle Insulin Syringe...

The Issue: Visible orange/ brown particulate on the needles of the 29g Hypodermic...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 10, 2013· Smiths Medical ASD, Inc.

Recalled Item: Jelco Smiths Medical Hypodermic Needle-Pro¿ Fixed Needle Insulin Syringe...

The Issue: Visible orange/ brown particulate on the needles of the 29g Hypodermic...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 10, 2013· Smiths Medical ASD, Inc.

Recalled Item: Jelco Smiths Medical Hypodermic Needle-Pro¿ Fixed Needle Insulin Syringe...

The Issue: Visible orange/ brown particulate on the needles of the 29g Hypodermic...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 9, 2013· Medtronic Xomed, Inc.

Recalled Item: Tray Surgical Recalled by Medtronic Xomed, Inc. Due to The firm will recall...

The Issue: The firm will recall and replace the identified instrument trays in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 8, 2013· Becton Dickinson & Co.

Recalled Item: PrepStain Tecan US-I. For use in the screening and detection Recalled by...

The Issue: PrepStain system rack setting was incorrectly entered on one PrepStain...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 8, 2013· Philips Healthcare Inc.

Recalled Item: Radiohead Access Point 1.4 GHz Radiohead Access Point Firmware versions:...

The Issue: IntelliVue Smart-hopping 1.4 GHz Access Point may experience unexpected...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 8, 2013· Stryker Howmedica Osteonics Corp.

Recalled Item: Stryker 1) Asnis III Cannulated Screw 4.0x40mm TL Recalled by Stryker...

The Issue: Stryker received a report that the length of the cannulated screw asnis III,...

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

Class II — Potential Health HazardOngoing