Ultra Seal Corporation recalls Cold Relief (acetaminophen 250 mg, guaifenesin 200mg, phenylephrine HCl 5 mg) 2 tablets per packet, Mfd. for First Aid D
Recalled February 9, 2022 · FDA recall D-0483-2022 · Ultra Seal
Hazard
cGMP deviations · FDA Class II
Units
7,858,690 packets
Sold at
Nationwide within the United States
Description
cGMP deviations
Product
Cold Relief (acetaminophen 250 mg, guaifenesin 200mg, phenylephrine HCl 5 mg) 2 tablets per packet, Mfd. for First Aid Direct, Mason, OH 45040, NDC 42961-112-03
Manufacturer(s)
Ultra Seal Corporation
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →