Ultra Seal Corporation recalls Extra Strength (ES) PAIN RELIEVER (acetaminophen 500 mg) 2 tablet packets, Manufactured by Ultratab Laboratories, Inc.
Recalled February 9, 2022 · FDA recall D-0469-2022 · Ultra Seal
Hazard
cGMP deviations · FDA Class II
Units
297,050 packets
Sold at
Nationwide within the United States
Description
cGMP deviations
Product
Extra Strength (ES) PAIN RELIEVER (acetaminophen 500 mg) 2 tablet packets, Manufactured by Ultratab Laboratories, Inc.
Manufacturer(s)
Ultra Seal Corporation
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →