Ultra Seal Corporation recalls Multi Symptom Cold Relief (acetaminophen 325 mg, Dextromethorphan HBr 15mg, Guaifenesin 200mg, Phenylephrine HCl 5mg) ta
Recalled February 9, 2022 · FDA recall D-0478-2022 · Ultra Seal
Hazard
cGMP deviations · FDA Class II
Units
673,160 packets
Sold at
Nationwide within the United States
Description
cGMP deviations
Product
Multi Symptom Cold Relief (acetaminophen 325 mg, Dextromethorphan HBr 15mg, Guaifenesin 200mg, Phenylephrine HCl 5mg) tablets, 2-count packets, Dist. by Honeywell Safety Products USA, Smithfield, RI 02917
Manufacturer(s)
Ultra Seal Corporation
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →