Ultra Seal Corporation recalls DILOTAB II, SINUS AND COLD RELIEF NON DROWSY (acetaminophen 325 mg, Phenylephrine HCl 5 mg) 2 tablet packets, Dist. by Z
Recalled February 9, 2022 · FDA recall D-0490-2022 · Ultra Seal
Hazard
cGMP deviations · FDA Class II
Units
2,685,700 packets
Sold at
Nationwide within the United States
Description
cGMP deviations
Product
DILOTAB II, SINUS AND COLD RELIEF NON DROWSY (acetaminophen 325 mg, Phenylephrine HCl 5 mg) 2 tablet packets, Dist. by ZEE Medical Distributors, LLC Mason, OH 45040, NDC 42961-052-03
Manufacturer(s)
Ultra Seal Corporation
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →