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 2606126080 of 28,688 recalls

Medical DeviceJuly 8, 2013· Medtronic Inc. Cardiac Rhythm Disease Management

Recalled Item: Medtronic Mullins Transseptal Adult 7F Recalled by Medtronic Inc. Cardiac...

The Issue: Medtronic identified a specific labeling issue for specific lots of Mullins...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 8, 2013· Sorin Group USA, Inc.

Recalled Item: Edwards Lifesciences Suction Wand Model S099B Recalled by Sorin Group USA,...

The Issue: Sorin Group is recalling certain lots of Edwards Lifesciences Suction Wand...

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 AG. For use in the screening and detection of cervical cancer....

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· Becton Dickinson & Co.

Recalled Item: PrepStain Tecan US-II. 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 5, 2013· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance CT 6 Recalled by Philips Medical Systems (Cleveland) Inc Due to...

The Issue: The patient support may move in an unintended manner if the footswitch cover...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 5, 2013· Radiometer America Inc

Recalled Item: pCO2 D788 Membranes. Distributed by Radiometer America Recalled by...

The Issue: RADIOMETER has become aware that some D788 pCO2 membranes can cause biased...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 3, 2013· Medtronic MiniMed

Recalled Item: Medtronic MiniMed Paradigm Reservoirs Recalled by Medtronic MiniMed Due to...

The Issue: Medtronic is recalling certain lots of Medtronic MiniMed Paradigm Reservoirs...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 2, 2013· Ecolab Inc

Recalled Item: MICROTEK(TM) MEDICAL BUR HOLE LATEX PROBE COVER WITH GEL Recalled by Ecolab...

The Issue: Certain lots of these Bur Hole Probe Covers did not undergo endotoxin (LAL)...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 2, 2013· Elekta, Inc.

Recalled Item: Monaco RTP System Radiation treatment planning Recalled by Elekta, Inc. Due...

The Issue: Upgrade installation script is designed to overwrite the same pouch files in...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 2, 2013· Ecolab Inc

Recalled Item: MICROTEK(TM) MEDICAL BUR HOLE LATEX FREE PROBE COVER W/ GEL Recalled by...

The Issue: Certain lots of these Bur Hole Probe Covers did not undergo endotoxin (LAL)...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 2, 2013· Ecolab Inc

Recalled Item: MICROTEK(TM) MEDICAL BUR HOLE LATEX FREE PROBE COVER WITH GEL Recalled by...

The Issue: Certain lots of these Bur Hole Probe Covers did not undergo endotoxin (LAL)...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 2, 2013· Ecolab Inc

Recalled Item: Vital CARE(TM) REPS INC. ULTRASOUND PROBE COVER Recalled by Ecolab Inc Due...

The Issue: Certain lots of these Bur Hole Probe Covers did not undergo endotoxin (LAL)...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 2, 2013· Stryker Howmedica Osteonics Corp.

Recalled Item: Stryker Howmedica Osteonics Triathlon tibial alignment ankle clamp...

The Issue: Cracks or fracture of the Triathlon Tibial Alignment Ankle Clamp, an instrument.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 2, 2013· Ecolab Inc

Recalled Item: MICROTEK(TM) MEDICAL BUR HOLE LATEX FREE PROBE COVER Recalled by Ecolab Inc...

The Issue: Certain lots of these Bur Hole Probe Covers did not undergo endotoxin (LAL)...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 2, 2013· Ecolab Inc

Recalled Item: MICROTEK(TM) MEDICAL BUR HOLE LATEX PROBE COVER W/ GEL Recalled by Ecolab...

The Issue: Certain lots of these Bur Hole Probe Covers did not undergo endotoxin (LAL)...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 1, 2013· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Dimension Tacrolimus Flex reagent cartridge (DF107) and Dimension TACR CAL...

The Issue: Siemens initiated a recall due to confirmed complaints of low patient sample...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 1, 2013· Stryker Instruments Div. of Stryker Corporation

Recalled Item: CORE Universal Driver 99 Rx Only This drill Recalled by Stryker Instruments...

The Issue: The safety margin values detailed in the Engineering Design were entered...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 1, 2013· Stryker Instruments Div. of Stryker Corporation

Recalled Item: Stryker TPS Universal Driver 99 Rx Recalled by Stryker Instruments Div. of...

The Issue: The safety margin values detailed in the Engineering Design were entered...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 1, 2013· Stryker Instruments Div. of Stryker Corporation

Recalled Item: RemB Electric Universal Driver For use with the Recalled by Stryker...

The Issue: The safety margin values detailed in the Engineering Design were entered...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 1, 2013· Iradimed Corporation

Recalled Item: MRidium 1145 Dose Reduction System (DERS) drug library kit. (This Recalled...

The Issue: The Dose Error Reduction System (DERS) can indicate an incorrect recommended...

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

Class I — Serious Health HazardOngoing