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. 1,865 recalls have been distributed to South Carolina in the last 12 months.

51,854 total recalls
1,865 in last 12 months

Showing 2750127520 of 51,854 recalls

Medical DeviceApril 16, 2018· St Jude Medical Inc.

Recalled Item: Merlin PCS programmer (Model # 3650) Recalled by St Jude Medical Inc. Due to...

The Issue: The firm is releasing new firmware for high voltage implantable cardiac...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 16, 2018· St Jude Medical Inc.

Recalled Item: Unify Recalled by St Jude Medical Inc. Due to The firm is releasing new...

The Issue: The firm is releasing new firmware for high voltage implantable cardiac...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 16, 2018· St Jude Medical Inc.

Recalled Item: Fortify Recalled by St Jude Medical Inc. Due to The firm is releasing new...

The Issue: The firm is releasing new firmware for high voltage implantable cardiac...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 16, 2018· St Jude Medical Inc.

Recalled Item: Fortify Assura Recalled by St Jude Medical Inc. Due to The firm is releasing...

The Issue: The firm is releasing new firmware for high voltage implantable cardiac...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 16, 2018· St Jude Medical Inc.

Recalled Item: Unify Quadra Recalled by St Jude Medical Inc. Due to The firm is releasing...

The Issue: The firm is releasing new firmware for high voltage implantable cardiac...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 16, 2018· St Jude Medical Inc.

Recalled Item: Quadra Assura MP Recalled by St Jude Medical Inc. Due to The firm is...

The Issue: The firm is releasing new firmware for high voltage implantable cardiac...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 16, 2018· St Jude Medical Inc.

Recalled Item: Promote Recalled by St Jude Medical Inc. Due to The firm is releasing new...

The Issue: The firm is releasing new firmware for high voltage implantable cardiac...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 16, 2018· St Jude Medical Inc.

Recalled Item: Ellipse Recalled by St Jude Medical Inc. Due to The firm is releasing new...

The Issue: The firm is releasing new firmware for high voltage implantable cardiac...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 16, 2018· St Jude Medical Inc.

Recalled Item: Current Recalled by St Jude Medical Inc. Due to The firm is releasing new...

The Issue: The firm is releasing new firmware for high voltage implantable cardiac...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 16, 2018· St Jude Medical Inc.

Recalled Item: Promote Quadra Recalled by St Jude Medical Inc. Due to The firm is releasing...

The Issue: The firm is releasing new firmware for high voltage implantable cardiac...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 16, 2018· St Jude Medical Inc.

Recalled Item: Unify Assura Recalled by St Jude Medical Inc. Due to The firm is releasing...

The Issue: The firm is releasing new firmware for high voltage implantable cardiac...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 16, 2018· St Jude Medical Inc.

Recalled Item: Quadra Assura Recalled by St Jude Medical Inc. Due to The firm is releasing...

The Issue: The firm is releasing new firmware for high voltage implantable cardiac...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 16, 2018· Bard Peripheral Vascular Inc

Recalled Item: BARD PERIPHERAL VASCULAR SEEKER(R) Crossing Support Catheter Recalled by...

The Issue: Device is at risk of having detectable levels of bacterial endotoxin present...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 16, 2018· Bard Peripheral Vascular Inc

Recalled Item: BARD PERIPHERAL VASCULAR SEEKER(R) Crossing Support Catheter Recalled by...

The Issue: Device is at risk of having detectable levels of bacterial endotoxin present...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 16, 2018· Cook Inc.

Recalled Item: Advance¿ 35LP Low-Profile PTA Balloon Dilatation Catheter Recalled by Cook...

The Issue: Incorrect product labeling. Product labeled as 6mm x 2cm balloon are...

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

Class II — Potential Health HazardOngoing
DrugApril 13, 2018· Boiron Inc.

Recalled Item: Calendula Cream Recalled by Boiron Inc. Due to Labeling: Labeling Error on...

The Issue: Labeling: Labeling Error on Declared Strength; The outer carton (secondary...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
FoodApril 13, 2018· ROSE ACRE FARM

Recalled Item: Shell Eggs packaged in quantities and styles of pack (plastic and pulp...

The Issue: Shell eggs have the potential to be contaminated with Salmonella Braenderup.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodApril 13, 2018· Cheezwhse/Com

Recalled Item: Formagere de la Brie brand Recalled by Cheezwhse/Com Due to Potential...

The Issue: Product may be contaminated with Listeria monocytogenes.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
Medical DeviceApril 13, 2018· St Jude Medical, Cardiac Rhythm Management Division

Recalled Item: Merlin PCS Programmer software model 3330 Recalled by St Jude Medical,...

The Issue: Devices inappropriately displayed a low battery indicator determined to be...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2018· CareFusion 303, Inc.

Recalled Item: Alaris Pump Recalled by CareFusion 303, Inc. Due to The bezel manufacturing...

The Issue: The bezel manufacturing process for the FR-110 plastic may have resulted in...

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

Class I — Serious Health HazardOngoing