Ultra Seal Corporation recalls Cold Relief Severe Pain/Cough (acetaminophen 325mg, Dextromethorphan HBr 15mg, Guaifenesin 200mg, phenylephrine HCl 5mg)
Recalled February 9, 2022 · FDA recall D-0480-2022 · Ultra Seal
Hazard
cGMP deviations · FDA Class II
Units
227,010 packets
Sold at
Nationwide within the United States
Description
cGMP deviations
Product
Cold Relief Severe Pain/Cough (acetaminophen 325mg, Dextromethorphan HBr 15mg, Guaifenesin 200mg, phenylephrine HCl 5mg), 2-tablet packets, Manufactured for Select Corporation, Carrollton, TX 75007
Manufacturer(s)
Ultra Seal Corporation
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →