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. 973 recalls have been distributed to South Carolina in the last 12 months.
Showing 38601–38620 of 51,854 recalls
Recalled Item: Equaline Original Prescription Strength Recalled by Ohm Laboratories, Inc....
The Issue: Superpotent Drug: Out Of Specification (OOS) result for Assay.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Discount Drug Mart Food Fair Recalled by Ohm Laboratories, Inc. Due to...
The Issue: Superpotent Drug: Out Of Specification (OOS) result for Assay.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Up&Up loratadine orally disintegrating tablets Recalled by Ohm Laboratories,...
The Issue: Superpotent Drug: Out Of Specification (OOS) result for Assay.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Rite Aid Pharmacy loratadine orally disintegrating tablets USP Recalled by...
The Issue: Superpotent Drug: Out Of Specification (OOS) result for Assay.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ohm Loratadine Orally Disintegrating Tablets Recalled by Ohm Laboratories,...
The Issue: Superpotent Drug: Out Of Specification (OOS) result for Assay.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Health Mart Pharmacy loratadine orally disintegrating tablets Recalled by...
The Issue: Superpotent Drug: Out Of Specification (OOS) result for Assay.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: QC Quality Choice Loratadine Orally Disintegrating Tablets Recalled by Ohm...
The Issue: Superpotent Drug: Out Of Specification (OOS) result for Assay.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Hydralazine Hydrochloride Injection Recalled by Fresenius Kabi USA, LLC Due...
The Issue: Incorrect Expiration Date: The "11/06" expiration date printed on the tray...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Health Best Choice Care Recalled by Ohm Laboratories, Inc. Due to...
The Issue: Superpotent Drug: Out Of Specification (OOS) result for Assay.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Daytrana (methylphenidate transdermal system) Recalled by Noven...
The Issue: Defective Delivery System: Out of specification for z-statistic related to...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Transonic Flow Probe Recalled by Transonic Systems Inc Due to Software...
The Issue: Software defect; programming errors in the blood flow probes EPROM....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Transonic Flow Probe Recalled by Transonic Systems Inc Due to Software...
The Issue: Software defect; programming errors in the blood flow probes EPROM....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Transonic Flow Probe Recalled by Transonic Systems Inc Due to Software...
The Issue: Software defect; programming errors in the blood flow probes EPROM....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Transonic Flow Probe Recalled by Transonic Systems Inc Due to Software...
The Issue: Software defect; programming errors in the blood flow probes EPROM....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CIDEX Activated Dialdehyde Solution Recalled by Advanced Sterilization...
The Issue: Advanced Sterilization Products (ASP) is recalling the CIDEX Activated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Transonic Flow Probe Recalled by Transonic Systems Inc Due to Software...
The Issue: Software defect; programming errors in the blood flow probes EPROM....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Centaur¿ Folate Ascorbic Acid/Ascorbic Acid Diluent Recalled by...
The Issue: Low red blood cell control recoveries and low results for red blood cell...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Transonic Flow Probe Recalled by Transonic Systems Inc Due to Software...
The Issue: Software defect; programming errors in the blood flow probes EPROM....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Transonic Flow Probe Recalled by Transonic Systems Inc Due to Software...
The Issue: Software defect; programming errors in the blood flow probes EPROM....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Transonic Flow Probe Recalled by Transonic Systems Inc Due to Software...
The Issue: Software defect; programming errors in the blood flow probes EPROM....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.