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. 2,672 recalls have been distributed to South Carolina in the last 12 months.

51,854 total recalls
2,672 in last 12 months

Showing 1220112220 of 51,854 recalls

DrugJuly 11, 2022· Hikma Pharmaceuticals USA Inc.

Recalled Item: Lorazepam Injection Recalled by Hikma Pharmaceuticals USA Inc. Due to Failed...

The Issue: Failed Impurities/Degradation Specifications: Out-of-specification results...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 11, 2022· Hikma Pharmaceuticals USA Inc.

Recalled Item: Lorazepam Injection Recalled by Hikma Pharmaceuticals USA Inc. Due to Failed...

The Issue: Failed Impurities/Degradation Specifications: Out-of-specification results...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 11, 2022· Hikma Pharmaceuticals USA Inc.

Recalled Item: Lorazepam Injection Recalled by Hikma Pharmaceuticals USA Inc. Due to Failed...

The Issue: Failed Impurities/Degradation Specifications: Out-of-specification results...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJuly 11, 2022· WISSNER-BOSSERHOFF GMBH

Recalled Item: SafeControl handset (a component of the Sentida bed which moves Recalled by...

The Issue: When the handset is disconnected from the power mains, and mains operation...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 11, 2022· Synapse Biomedical Inc

Recalled Item: NeuRx Diaphragm Pacing System (NeuRx DPS) External Pulse Generator (EPG)...

The Issue: Due to a defect identified on the EPG controller printed circuit board...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 8, 2022· Oculus Optikgeraete GMBH

Recalled Item: Pentacam AXL Recalled by Oculus Optikgeraete GMBH Due to Due to a software...

The Issue: Due to a software issue, IOL calculator printout often does not accurately...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 8, 2022· Oculus Optikgeraete GMBH

Recalled Item: Pentacam AXL Wave . Used to image the anterior segment of the eye. Recalled...

The Issue: Due to a software issue, IOL calculator printout often does not accurately...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 8, 2022· Oculus Optikgeraete GMBH

Recalled Item: Pentacam HR . Used to image the anterior segment of the eye. Recalled by...

The Issue: Due to a software issue, IOL calculator printout often does not accurately...

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

Class II — Potential Health HazardOngoing
DrugJuly 7, 2022· Apotex Corp.

Recalled Item: Aripiprazole Tablets Recalled by Apotex Corp. Due to Failed dissolution...

The Issue: Failed dissolution specifications: OOS for dissolution at the 12-month...

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

Class II — Potential Health HazardOngoing
Refund
FoodJuly 7, 2022· Refresco Beverages US Inc

Recalled Item: Clear American brand "Strawberry Punch Snow Cone" flavored sparkling water...

The Issue: The product may contain trace amounts of coconut, which is not declared on...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJuly 7, 2022· Olympus Corporation of the Americas

Recalled Item: ShockPulse-SE Lithotripsy Generator Model/Serial: SPL-S Recalled by Olympus...

The Issue: Mis-wired component-the improperly wired component can result in additional...

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

Class II — Potential Health HazardOngoing
FoodJuly 6, 2022· Southeast Processing Ltd

Recalled Item: Yellow Squash sold as Bulk Recalled by Southeast Processing Ltd Due to...

The Issue: Finished product samples of half moon sliced yellow squash reported positive...

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

Class I — Serious Health HazardOngoing
Refund
DrugJuly 5, 2022· Mylan Pharmaceuticals Inc

Recalled Item: Insulin Glargine (Insulin glargine-yfgn) Injection Recalled by Mylan...

The Issue: Labeling: Missing label: Label missing from some prefilled pens.

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

Class I — Serious Health HazardOngoing
Refund
FoodJuly 5, 2022· TOVALA

Recalled Item: Tovala Gochujang-Glazed Pork Chop Bowl meal No.9-A Recalled by TOVALA Due to...

The Issue: Product contains undeclared peanut

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

Class I — Serious Health HazardOngoing
Refund
FoodJuly 5, 2022· TOVALA

Recalled Item: Tovala Gochujang-Glazed Salmon Bowl meal No.18-A Recalled by TOVALA Due to...

The Issue: Product contains undeclared peanut

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJuly 5, 2022· Zap Surgical Systems

Recalled Item: ZAP-X Radiosurgery System Recalled by Zap Surgical Systems Due to Software...

The Issue: Software issue identified in cases of initial patient setup with large...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 4, 2022· Medicina Uk Ltd

Recalled Item: Medicina Oral Tip Syringe 0.5ml Code: OT005 Recalled by Medicina Uk Ltd Due...

The Issue: Plunger component has been manufactured with an unapproved material...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 4, 2022· Medicina Uk Ltd

Recalled Item: Medicina ENFit 1ml Reusable Low Dose Enteral Syringe Code: LHE01LD Recalled...

The Issue: Plunger component has been manufactured with an unapproved material...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 4, 2022· Medicina Uk Ltd

Recalled Item: Medicina Oral Tip Syringe 2.5ml Code: OT25 Recalled by Medicina Uk Ltd Due...

The Issue: Plunger component has been manufactured with an unapproved material...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 4, 2022· Medicina Uk Ltd

Recalled Item: Medicina ENFit 5ml Reusable Enteral Syringe Code: LHE05 Recalled by Medicina...

The Issue: Plunger component has been manufactured with an unapproved material...

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

Class II — Potential Health HazardOngoing