Class II Recall

Ultra Seal Corporation

Product
Cold Relief Severe Pain/Cough (acetaminophen 325mg, Dextromethorphan HBr 15mg, Guaifenesin 200mg, phenylephrine HCl 5mg), 2-tablet packets, Manufactured for Select Corporation, Carrollton, TX 75007
Reason
cGMP deviations
Classification
Class II
Status
Terminated
Lot
Lot #: AK9436, Exp. Date 01/2022
Date
Disclaimer: This tool indexes published US FDA drug-enforcement recall records from all countries, limited to the latest five years. A company or product not appearing here is not proof that it is compliant, approved, safe, or free of FDA action.
Ultra Seal Corporation — Class II Recall | MedicineWatch US