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. 1,077 recalls have been distributed to South Carolina in the last 12 months.

51,854 total recalls
1,077 in last 12 months

Showing 11661–11680 of 51,854 recalls

Medical DeviceSeptember 28, 2022· Cardinal Health 200, LLC

Recalled Item: Cardinal Health GEL PACK REUSABLE Recalled by Cardinal Health 200, LLC Due...

The Issue: Users are being informed that the product should not be used on...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 28, 2022· Cardinal Health 200, LLC

Recalled Item: Cardinal Health INSULATED GEL PACK REUSABLE Recalled by Cardinal Health 200,...

The Issue: Users are being informed that the product should not be used on...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 28, 2022· Biokit, S.A.

Recalled Item: biokitHSV-2 Rapid Test Recalled by Biokit, S.A. Due to HSV-2 rapid test may...

The Issue: HSV-2 rapid test may report false positive results.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 28, 2022· Cardinal Health 200, LLC

Recalled Item: Cardinal Health GEL PACK REUSABLE Recalled by Cardinal Health 200, LLC Due...

The Issue: Users are being informed that the product should not be used on...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 28, 2022· Cardinal Health 200, LLC

Recalled Item: Cardinal Health HOT AND COLD GEL PACK REUSABLE Recalled by Cardinal Health...

The Issue: Users are being informed that the product should not be used on...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 28, 2022· Cardinal Health 200, LLC

Recalled Item: Cardinal Health INSULATED GEL PACK REUSABLE Recalled by Cardinal Health 200,...

The Issue: Users are being informed that the product should not be used on...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 28, 2022· Covidien, LP

Recalled Item: Endo Stitch V-Loc PBT Non-Absorbable Reload Recalled by Covidien, LP Due to...

The Issue: Medtronic has received 210 reports of needles breaking during endoscopic...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 28, 2022· iRhythm Technologies, Inc.

Recalled Item: Zio AT Clinical Manual Recalled by iRhythm Technologies, Inc. Due to...

The Issue: Ambulatory ECG monitoring system labeling update: 1) Clinically actionable...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 28, 2022· Covidien, LP

Recalled Item: Endo Stitch V-Loc 180 Absorbable Reload Recalled by Covidien, LP Due to...

The Issue: Medtronic has received 210 reports of needles breaking during endoscopic...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 28, 2022· Cardinal Health 200, LLC

Recalled Item: Cardinal Health INSULATED GEL PACK REUSABLE Recalled by Cardinal Health 200,...

The Issue: Users are being informed that the product should not be used on...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 27, 2022· Synthes (USA) Products LLC

Recalled Item: SPEED 9X10X10mm Continuous Compression Implant Recalled by Synthes (USA)...

The Issue: The subject products are being recalled because they contain the incorrect...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 27, 2022· Synthes (USA) Products LLC

Recalled Item: SPEED 15X12X12mm Continuous Compression Implant Recalled by Synthes (USA)...

The Issue: The subject products are being recalled because they contain the incorrect...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 27, 2022· Synthes (USA) Products LLC

Recalled Item: SPEEDSHIFT20x20x20 Offset 10mm Implant Drill Kit Recalled by Synthes (USA)...

The Issue: The subject products are being recalled because they contain the incorrect...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 27, 2022· Synthes (USA) Products LLC

Recalled Item: DePuy Synthes Hammertoe Continuous Compression Implants Recalled by Synthes...

The Issue: The subject products are being recalled because they contain the incorrect...

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

Class II — Potential Health HazardOngoing
DrugSeptember 26, 2022· AuroMedics Pharma LLC

Recalled Item: Acyclovir Sodium Injection Recalled by AuroMedics Pharma LLC Due to Presence...

The Issue: Presence of Particulate Matter: Customer complaint for a dark red, brown and...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 26, 2022· AuroMedics Pharma LLC

Recalled Item: Tranexamic Acid Injection Recalled by AuroMedics Pharma LLC Due to Presence...

The Issue: Presence of Particulate Matter: Piece of metal found in a vial

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

Class III — Low RiskOngoing
Refund
Medical DeviceSeptember 23, 2022· LumiraDx

Recalled Item: LumiraDx SARS-CoV-2 Antigen (Ag) Liquid Quality Control Kit Catalog #:...

The Issue: Assigned vial lot numbers for the incorrect type of product. SARS-CoV-2 &...

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

Class III — Low RiskOngoing
Medical DeviceSeptember 23, 2022· GAGA PRO LIGHTING EQUIPMENT CO.,

Recalled Item: GaGa Pro Lighting Equipment Co. Ltd. manufactures Class IV Laser Recalled by...

The Issue: GAGA Pro LLS systems was not in compliance with the FDA's Performance...

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

Class II — Potential Health HazardOngoing
FoodSeptember 23, 2022· Lyons Magnus LLC

Recalled Item: Lyons Ready Care Thickened Cranberry Honey Nectar packaged in combi-bloc...

The Issue: Indication of product spoilage

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

Class II — Potential Health HazardOngoing
Refund
FoodSeptember 23, 2022· Lyons Magnus LLC

Recalled Item: Lyons Ready Care Thickened Orange Juice packaged in combi-bloc multi...

The Issue: Indication of product spoilage

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

Class II — Potential Health HazardOngoing
Refund