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. 1,064 recalls have been distributed to South Carolina in the last 12 months.

51,854 total recalls
1,064 in last 12 months

Showing 15101–15120 of 28,688 recalls

Medical DeviceSeptember 27, 2018· Orthofix Srl

Recalled Item: ORTHOFIX Catalogue Number: Recalled by Orthofix Srl Due to As a result of...

The Issue: As a result of complaint investigations it was determined that batches of...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 27, 2018· Orthofix Srl

Recalled Item: ORTHOFIX Catalogue Number: Recalled by Orthofix Srl Due to As a result of...

The Issue: As a result of complaint investigations it was determined that batches of...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 27, 2018· Orthofix Srl

Recalled Item: ORTHOFIX Catalogue Number: Recalled by Orthofix Srl Due to As a result of...

The Issue: As a result of complaint investigations it was determined that batches of...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 27, 2018· Orthofix Srl

Recalled Item: ORTHOFIX Catalogue Number: Recalled by Orthofix Srl Due to As a result of...

The Issue: As a result of complaint investigations it was determined that batches of...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 27, 2018· Orthofix Srl

Recalled Item: ORTHOFIX Catalogue Number: Recalled by Orthofix Srl Due to As a result of...

The Issue: As a result of complaint investigations it was determined that batches of...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 27, 2018· Orthofix Srl

Recalled Item: ORTHOFIX Catalogue Number: Recalled by Orthofix Srl Due to As a result of...

The Issue: As a result of complaint investigations it was determined that batches of...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 27, 2018· Orthofix Srl

Recalled Item: ORTHOFIX Catalogue Number: Recalled by Orthofix Srl Due to As a result of...

The Issue: As a result of complaint investigations it was determined that batches of...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 27, 2018· Orthofix Srl

Recalled Item: ORTHOFIX Catalogue Number: Recalled by Orthofix Srl Due to As a result of...

The Issue: As a result of complaint investigations it was determined that batches of...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 27, 2018· Orthofix Srl

Recalled Item: ORTHOFIX Catalogue Number: Recalled by Orthofix Srl Due to As a result of...

The Issue: As a result of complaint investigations it was determined that batches of...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 27, 2018· Orthofix Srl

Recalled Item: ORTHOFIX Catalogue Number: Recalled by Orthofix Srl Due to As a result of...

The Issue: As a result of complaint investigations it was determined that batches of...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 27, 2018· Orthofix Srl

Recalled Item: ORTHOFIX Catalogue Number: Recalled by Orthofix Srl Due to As a result of...

The Issue: As a result of complaint investigations it was determined that batches of...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 27, 2018· Orthofix Srl

Recalled Item: ORTHOFIX Catalogue Number: Recalled by Orthofix Srl Due to As a result of...

The Issue: As a result of complaint investigations it was determined that batches of...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 27, 2018· Orthofix Srl

Recalled Item: ORTHOFIX Catalogue Number: Recalled by Orthofix Srl Due to As a result of...

The Issue: As a result of complaint investigations it was determined that batches of...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 27, 2018· Orthofix Srl

Recalled Item: ORTHOFIX Catalogue Number: Recalled by Orthofix Srl Due to As a result of...

The Issue: As a result of complaint investigations it was determined that batches of...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 27, 2018· GE Healthcare, LLC

Recalled Item: Aisys Anesthesia System. Sold under the following product names: AISYS...

The Issue: Upgraded Aisys anesthesia devices and Aisys CS2 anesthesia devices with...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 27, 2018· GE Healthcare, LLC

Recalled Item: Aisys CS2 Anesthesia System. Sold under the following product names: AISYS...

The Issue: Upgraded Aisys anesthesia devices and Aisys CS2 anesthesia devices with...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 27, 2018· GE Healthcare, LLC

Recalled Item: Touchscreen display kit. Sold under the following product names: TOUCHSCREEN...

The Issue: Upgraded Aisys anesthesia devices and Aisys CS2 anesthesia devices with...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 26, 2018· Medtronic Navigation, Inc.

Recalled Item: StealthStation Cranial and Synergy Cranial Depth Gauge: StealthStation...

The Issue: An incorrect display of the Biopsy Depth Gauge graphical representation in...

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 26, 2018· Becton Dickinson & Company

Recalled Item: PCEA ASV Yellow Microbore Recalled by Becton Dickinson & Company Due to The...

The Issue: The products have the potential to leak between the connection of the male...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 26, 2018· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Atellica Sample Handler Prime. In vitro diagnostic testing of clinical...

The Issue: Multiple Issues Identified in Atellica Solution System Software in V 1.14.2...

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

Class II — Potential Health HazardOngoing