Ultra Seal Corporation recalls Maximum Strength Non Aspirin Pain Reliever/Fever Reducer (acetaminophen 500 mg) 2 tablet packets, Mfg. for: Advanced Fir
Recalled February 9, 2022 · FDA recall D-0467-2022 · Ultra Seal
Hazard
cGMP deviations · FDA Class II
Units
1,236,000 packets
Sold at
Nationwide within the United States
Description
cGMP deviations
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
Manufacturer(s)
Ultra Seal Corporation
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →