Ultra Seal Corporation recalls PAINAID BRF Back Relief Formula (acetaminophen 250 mg, caffeine 50 mg, Magnesium salicylate 290 mg) 2 tablet packets, Di
Recalled February 9, 2022 · FDA recall D-0493-2022 · Ultra Seal
Hazard
cGMP deviations · FDA Class II
Units
111,300 packets
Sold at
Nationwide within the United States
Description
cGMP deviations
Product
PAINAID BRF Back Relief Formula (acetaminophen 250 mg, caffeine 50 mg, Magnesium salicylate 290 mg) 2 tablet packets, Dist. by ZEE Medical Distributors, LLC Mason, OH 45040, NDC 42961-0003-00
Manufacturer(s)
Ultra Seal Corporation
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →