FDA Drug Recalls

Recalls / Class II

Class IID-0467-2022

Product

Maximum Strength Non Aspirin Pain Reliever/Fever Reducer (acetaminophen 500 mg) 2 tablet packets, Mfg. for: Advanced First Aid, Baltimore MD 21237, American Safety & First Aid, Osceola, IN 46561, NDC 67060-210-68

Affected lot / code info
Lot #: AK9495, Exp. Date 02/2022; AK9613, Exp. Date 05/2022

Why it was recalled

cGMP deviations

Recalling firm

Firm
Ultra Seal Corporation
Notification channel
Letter
Type
Voluntary: Firm initiated
Address
521 Main St, N/A, New Paltz, New York 12561-1609

Distribution

Quantity
1,236,000 packets
Distribution pattern
Nationwide within the United States

Timeline

Recall initiated
2022-01-24
FDA classified
2022-01-31
Posted by FDA
2022-02-09
Terminated
2023-10-16
Status
Terminated

Source: openFDA Drug Enforcement endpoint. Recall record D-0467-2022. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.