Class II Recall

Ultra Seal Corporation

Product
Regular Strength Pain Reliever (acetaminophen 110 mg, aspirin 162 mg, Caffeine 32.4 mg, Salicylamide 152 mg) 2 tablet packets, Mfg for Advanced First Aid, Baltimore, MD 21237, NDC 67060-0113-00
Reason
cGMP deviations
Classification
Class II
Status
Terminated
Lot
Lot #: AK9450, 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