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. 1,884 recalls have been distributed to South Carolina in the last 12 months.

51,854 total recalls
1,884 in last 12 months

Showing 2392123940 of 51,854 recalls

DrugApril 2, 2019· Anderson Compounding Pharmacy, Inc. DBA Anderson Compounding Pharmacy

Recalled Item: Heparin 10 Recalled by Anderson Compounding Pharmacy, Inc. DBA Anderson...

The Issue: Lack of sterility assurance.

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 2, 2019· Anderson Compounding Pharmacy, Inc. DBA Anderson Compounding Pharmacy

Recalled Item: Lidocaine 1%/Dextrose 12.5% (PF) Injection Recalled by Anderson Compounding...

The Issue: Lack of sterility assurance.

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 2, 2019· Anderson Compounding Pharmacy, Inc. DBA Anderson Compounding Pharmacy

Recalled Item: Atropine 0.01% Eye Drops Recalled by Anderson Compounding Pharmacy, Inc. DBA...

The Issue: Lack of sterility assurance.

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 2, 2019· Anderson Compounding Pharmacy, Inc. DBA Anderson Compounding Pharmacy

Recalled Item: Prostaglandin Tri-Mix 30:30:1 Injection Recalled by Anderson Compounding...

The Issue: Lack of sterility assurance.

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 2, 2019· Anderson Compounding Pharmacy, Inc. DBA Anderson Compounding Pharmacy

Recalled Item: Serum Tears 30% Drops Recalled by Anderson Compounding Pharmacy, Inc. DBA...

The Issue: Lack of sterility assurance.

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 2, 2019· Anderson Compounding Pharmacy, Inc. DBA Anderson Compounding Pharmacy

Recalled Item: Penicillin G 100 Recalled by Anderson Compounding Pharmacy, Inc. DBA...

The Issue: Lack of sterility assurance.

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 2, 2019· Anderson Compounding Pharmacy, Inc. DBA Anderson Compounding Pharmacy

Recalled Item: Testosterone Cypionate 250 mg/mL Sterile Injection Recalled by Anderson...

The Issue: Lack of sterility assurance.

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 2, 2019· Anderson Compounding Pharmacy, Inc. DBA Anderson Compounding Pharmacy

Recalled Item: Prostaglandin Tri-Mix 8.33:22.5:0.833 Injection Recalled by Anderson...

The Issue: Lack of sterility assurance.

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 2, 2019· Anderson Compounding Pharmacy, Inc. DBA Anderson Compounding Pharmacy

Recalled Item: Polyhexamethylene Biguanide 0.02% Ophthalmic Drops Recalled by Anderson...

The Issue: Lack of sterility assurance.

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 2, 2019· Anderson Compounding Pharmacy, Inc. DBA Anderson Compounding Pharmacy

Recalled Item: Phenylephrine 1 mg/mL Injection Recalled by Anderson Compounding Pharmacy,...

The Issue: Lack of sterility assurance.

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 2, 2019· Anderson Compounding Pharmacy, Inc. DBA Anderson Compounding Pharmacy

Recalled Item: HCG 20 Day Extra Strength Recalled by Anderson Compounding Pharmacy, Inc....

The Issue: Lack of sterility assurance.

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 2, 2019· Anderson Compounding Pharmacy, Inc. DBA Anderson Compounding Pharmacy

Recalled Item: Prostaglandin Quad-Mix 20:30:1:0.15 Injection Recalled by Anderson...

The Issue: Lack of sterility assurance.

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 2, 2019· Anderson Compounding Pharmacy, Inc. DBA Anderson Compounding Pharmacy

Recalled Item: Phenol 10% Injection Recalled by Anderson Compounding Pharmacy, Inc. DBA...

The Issue: Lack of sterility assurance.

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 2, 2019· Anderson Compounding Pharmacy, Inc. DBA Anderson Compounding Pharmacy

Recalled Item: Prostaglandin Tri-Mix 50:30:1 Recalled by Anderson Compounding Pharmacy,...

The Issue: Lack of sterility assurance.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceApril 1, 2019· Olympus Corporation of the Americas

Recalled Item: Olympus MAJ-209 Single Use Suction Valves Recalled by Olympus Corporation of...

The Issue: There is a potential for the single use suction valve to come apart and/or...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 1, 2019· Zimmer Biomet, Inc.

Recalled Item: Mobi-C 14mm Distraction Screw Recalled by Zimmer Biomet, Inc. Due to...

The Issue: Incorrect part description contained on an additional label placed on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 1, 2019· Teleflex Medical

Recalled Item: RUSCH LASERTUBE (Rubber) Recalled by Teleflex Medical Due to The firm...

The Issue: The firm received reports indicating that the laser guard foil partially...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 1, 2019· Teleflex Medical

Recalled Item: RUSCH LASERTUBE (Rubber) Recalled by Teleflex Medical Due to The firm...

The Issue: The firm received reports indicating that the laser guard foil partially...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 1, 2019· Teleflex Medical

Recalled Item: RUSCH LASERTUBE (Rubber) Recalled by Teleflex Medical Due to The firm...

The Issue: The firm received reports indicating that the laser guard foil partially...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 1, 2019· Teleflex Medical

Recalled Item: RUSCH LASERTUBE (Rubber) Recalled by Teleflex Medical Due to The firm...

The Issue: The firm received reports indicating that the laser guard foil partially...

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

Class II — Potential Health HazardOngoing