Ultra Seal Corporation recalls Pain & Sinus Reliever Pain Reliever/Nasal Decongestant (acetaminophen 500mg, Phenylephrine HCl 5mg) 2 tablet packets, Mf
Recalled February 9, 2022 · FDA recall D-0497-2022 · Ultra Seal
Hazard
cGMP deviations · FDA Class II
Units
887,000 packets
Sold at
Nationwide within the United States
Description
cGMP deviations
Product
Pain & Sinus Reliever Pain Reliever/Nasal Decongestant (acetaminophen 500mg, Phenylephrine HCl 5mg) 2 tablet packets, Mfg for Advanced First Aid, Baltimore, MD 21237, NDC 67060-194-68
Manufacturer(s)
Ultra Seal Corporation
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →