Ultra Seal Corporation recalls Headache & Congestion Sinus Relief (acetaminophen 250 mg, phenylephrine HCl 5 mg) 2 tablets per packet, Mfd. for First A
Recalled February 9, 2022 · FDA recall D-0484-2022 · Ultra Seal
Hazard
cGMP deviations · FDA Class II
Units
5,741,384 packets
Sold at
Nationwide within the United States
Description
cGMP deviations
Product
Headache & Congestion Sinus Relief (acetaminophen 250 mg, phenylephrine HCl 5 mg) 2 tablets per packet, Mfd. for First Aid Direct, Mason, OH 45040, NDC 42961-0206-02
Manufacturer(s)
Ultra Seal Corporation
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →