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. 2,723 recalls have been distributed to South Carolina in the last 12 months.

51,854 total recalls
2,723 in last 12 months

Showing 51815200 of 13,686 recalls

DrugNovember 8, 2019· Med Man Distribution, Inc.

Recalled Item: UP2 Recalled by Med Man Distribution, Inc. Due to Undeclared Sildenafil

The Issue: Marketed without an Approved NDA/ANDA: Product contains undeclared...

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

Class I — Serious Health HazardOngoing
Refund
DrugNovember 8, 2019· Washington Homeopathic Products, Inc.

Recalled Item: Cell Salts Combination 6X Tablets Recalled by Washington Homeopathic...

The Issue: CGMP Deviations: products were not manufactured under current good...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 8, 2019· Med Man Distribution, Inc.

Recalled Item: Bow & Arrow Recalled by Med Man Distribution, Inc. Due to Undeclared Sildenafil

The Issue: Marketed without an Approved NDA/ANDA: Product contains undeclared...

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

Class I — Serious Health HazardOngoing
Refund
DrugNovember 8, 2019· Washington Homeopathic Products, Inc.

Recalled Item: Calcarea Sulphurica 6X Tablets Recalled by Washington Homeopathic Products,...

The Issue: CGMP Deviations: products were not manufactured under current good...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 8, 2019· Washington Homeopathic Products, Inc.

Recalled Item: Silicea 6X Tablets Recalled by Washington Homeopathic Products, Inc. Due to...

The Issue: CGMP Deviations: products were not manufactured under current good...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 8, 2019· Washington Homeopathic Products, Inc.

Recalled Item: Ferrum Phosphoricum 6X Tablets Recalled by Washington Homeopathic Products,...

The Issue: CGMP Deviations: products were not manufactured under current good...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 8, 2019· Washington Homeopathic Products, Inc.

Recalled Item: Kali Sulphuricum 6X Tablets Recalled by Washington Homeopathic Products,...

The Issue: CGMP Deviations: products were not manufactured under current good...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 6, 2019· AuroMedics Pharma LLC

Recalled Item: Ranitidine Syrup (Ranitidine Oral Solution Recalled by AuroMedics Pharma LLC...

The Issue: CGMP Deviations: N-nitrosodimethylamine (NDMA) has been detected in...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 6, 2019· AuroMedics Pharma LLC

Recalled Item: Aurobindo Ranitidine Capsules 150 mg Recalled by AuroMedics Pharma LLC Due...

The Issue: CGMP Deviations: N-nitrosodimethylamine (NDMA) has been detected in...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 6, 2019· AuroMedics Pharma LLC

Recalled Item: Aurobindo Ranitidine Caspules 150 mg Recalled by AuroMedics Pharma LLC Due...

The Issue: CGMP Deviations: N-nitrosodimethylamine (NDMA) has been detected in...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 6, 2019· AuroMedics Pharma LLC

Recalled Item: DG Health Acid Reducer Ranitidine Tablets 150 mg Recalled by AuroMedics...

The Issue: CGMP Deviations: N-nitrosodimethylamine (NDMA) has been detected in...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 6, 2019· AuroMedics Pharma LLC

Recalled Item: Aurobindo Ranitidine Capsules 300 mg Recalled by AuroMedics Pharma LLC Due...

The Issue: CGMP Deviations: N-nitrosodimethylamine (NDMA) has been detected in...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 1, 2019· American Health Packaging

Recalled Item: Ranitidine Syrup (Ranitidine Oral Solution USP) Recalled by American Health...

The Issue: CGMP Deviations: Presence of NDMA impurity detected in product.

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 1, 2019· KVK-Tech, Inc.

Recalled Item: Hydrocodone Bitartrate and Homatropine Methlybromide Oral Solution 5 mg/1.5...

The Issue: Presence of Foreign Substance: Black particles were found in the lots during...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 31, 2019· Fagron, Inc

Recalled Item: LETS GEL KIT Convenience Pack (To prepare 100 mL LETS GEL) Recalled by...

The Issue: Microbial contamination of non-sterile product.

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 30, 2019· Avantor Performance Materials Inc

Recalled Item: Potassium Phosphate Recalled by Avantor Performance Materials Inc Due to...

The Issue: Failed Stability Specifications: Product exceeds compendia and firm's...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 28, 2019· Lannett Company, Inc.

Recalled Item: Lannett Ranitidine Syrup (Ranitidine Oral Solution Recalled by Lannett...

The Issue: CGMP Deviations: Presence of NDMA impurity detected in product.

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 25, 2019· Novitium Pharma LLC

Recalled Item: Novitium Pharma Ranitidine Capsules 150 mg 500 capsules Rx Only Recalled by...

The Issue: CGMP Deviations: Presence of NDMA impurity detected in product.

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 25, 2019· Novitium Pharma LLC

Recalled Item: Novitium Pharma Ranitidine Capsules 150 mg 60 capsules Rx Only Recalled by...

The Issue: CGMP Deviations: Presence of NDMA impurity detected in product.

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 25, 2019· Novitium Pharma LLC

Recalled Item: Novitium Pharma Ranitidine Capsules 300 mg 30 capsules Rx Only Recalled by...

The Issue: CGMP Deviations: Presence of NDMA impurity detected in product.

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

Class II — Potential Health HazardOngoing
Refund