Class II Recall

Ultra Seal Corporation

Product
FEM-PRIN MENSTRUAL RELIEF (acetaminophen 325 mg, pamabrom 25mg) tablets, 2-count packets, Manufactured for: HARTHealth Seattle, WA 98124
Reason
cGMP deviations
Classification
Class II
Status
Terminated
Lot
Lot #: AK9695, Exp. Date 07/2022
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