Ultra Seal Corporation recalls COLD TERMINATOR decongestant/cold relief (acetaminophen 325 mg, Guaifenesin 200mg, 5.0 Phenylephrine HCl) 2 tablet packe
Recalled February 9, 2022 · FDA recall D-0487-2022 · Ultra Seal
Hazard
cGMP deviations · FDA Class II
Units
226,400 packets
Sold at
Nationwide within the United States
Description
cGMP deviations
Product
COLD TERMINATOR decongestant/cold relief (acetaminophen 325 mg, Guaifenesin 200mg, 5.0 Phenylephrine HCl) 2 tablet packets, Manufactured for: Tellus Medical Products, Carlsbad, CA 92011, NDC 69103-2556
Manufacturer(s)
Ultra Seal Corporation
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →