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. 2,583 recalls have been distributed to South Carolina in the last 12 months.

51,854 total recalls
2,583 in last 12 months

Showing 1806118080 of 28,688 recalls

Medical DeviceJune 5, 2017· Zimmer Biomet, Inc.

Recalled Item: M/DN Intramedullary Fixation Humeral Guide Wire - Smooth 2.4 mm Recalled by...

The Issue: The design verification for the previous packaging configuration G928 does...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 5, 2017· Angiodynamics, Inc.

Recalled Item: Accu2i pMTA Applicator Recalled by Angiodynamics, Inc. Due to The firm is...

The Issue: The firm is recalling product that has the potential to not function during...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 5, 2017· Angiodynamics, Inc.

Recalled Item: Accu2i pMTA Applicator Recalled by Angiodynamics, Inc. Due to The firm is...

The Issue: The firm is recalling product that has the potential to not function during...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 5, 2017· Angiodynamics, Inc.

Recalled Item: Accu2i pMTA Applicator Recalled by Angiodynamics, Inc. Due to The firm is...

The Issue: The firm is recalling product that has the potential to not function during...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 5, 2017· Zimmer Biomet, Inc.

Recalled Item: Zimmer Natural Nail System Tear Drop Guide Wire 2.4 mm Diameter Recalled by...

The Issue: The design verification for the previous packaging configuration G928 does...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 5, 2017· Zimmer Biomet, Inc.

Recalled Item: Lateral Troch Plate Full Crimp - 254mm Recalled by Zimmer Biomet, Inc. Due...

The Issue: Possibility that the patient label inside the product box was incorrectly...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 5, 2017· Zimmer Biomet, Inc.

Recalled Item: RED SEXP DSTL FEM 19CM RT ASSY Recalled by Zimmer Biomet, Inc. Due to...

The Issue: Possibility that the patient label inside the product box was incorrectly...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 2, 2017· Sterilmed Inc

Recalled Item: St. Jude Medical. Agilis NxT Steerable Introducer: B1-Directional Recalled...

The Issue: Inadequate seal due to lack of adhesive glue

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 2, 2017· St. Jude Medical, Inc.

Recalled Item: Infinity 7 Recalled by St. Jude Medical, Inc. Due to The firm discovered a...

The Issue: The firm discovered a risk of loss of Neuromodulation therapy due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 2, 2017· St. Jude Medical, Inc.

Recalled Item: Proclaim 5 Elite Recalled by St. Jude Medical, Inc. Due to The firm...

The Issue: The firm discovered a risk of loss of Neuromodulation therapy due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 2, 2017· C.R. Bard, Inc.

Recalled Item: BARD DISPOZ-A-BAG Leg Bag with Flip-Flo Valve with Drain Extension Recalled...

The Issue: Customer complaint of a cut in the side of the leg bag, indicating a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 2, 2017· St. Jude Medical, Inc.

Recalled Item: Infinity 5 Recalled by St. Jude Medical, Inc. Due to The firm discovered a...

The Issue: The firm discovered a risk of loss of Neuromodulation therapy due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 2, 2017· St. Jude Medical, Inc.

Recalled Item: Infinity 7 Recalled by St. Jude Medical, Inc. Due to The firm discovered a...

The Issue: The firm discovered a risk of loss of Neuromodulation therapy due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 2, 2017· St. Jude Medical, Inc.

Recalled Item: Infinity 5 Recalled by St. Jude Medical, Inc. Due to The firm discovered a...

The Issue: The firm discovered a risk of loss of Neuromodulation therapy due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 2, 2017· St. Jude Medical, Inc.

Recalled Item: Proclaim 7 Elite Recalled by St. Jude Medical, Inc. Due to The firm...

The Issue: The firm discovered a risk of loss of Neuromodulation therapy due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 1, 2017· Shippert Medical Technologies

Recalled Item: Tissu-Trans Filtron 250 Recalled by Shippert Medical Technologies Due to...

The Issue: Seal integrity of the Tissu-Trans product sterile packages cannot be assured.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 1, 2017· Shippert Medical Technologies

Recalled Item: Tissu-Trans Filtron 1000 Recalled by Shippert Medical Technologies Due to...

The Issue: Seal integrity of the Tissu-Trans product sterile packages cannot be assured.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 1, 2017· Shippert Medical Technologies

Recalled Item: Tissu-Trans Filtron 2000 Recalled by Shippert Medical Technologies Due to...

The Issue: Seal integrity of the Tissu-Trans product sterile packages cannot be assured.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 1, 2017· Shippert Medical Technologies

Recalled Item: Tissu-Trans Filtron 100 Recalled by Shippert Medical Technologies Due to...

The Issue: Seal integrity of the Tissu-Trans product sterile packages cannot be assured.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 1, 2017· Shippert Medical Technologies

Recalled Item: Tissu-Trans SFILL 360 Recalled by Shippert Medical Technologies Due to Seal...

The Issue: Seal integrity of the Tissu-Trans product sterile packages cannot be assured.

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

Class II — Potential Health HazardOngoing