Ultra Seal Corporation recalls Legatrin PM Pain Reliever/Sleep Aid (acetaminophen 500 mg, diphenhydramine HCl 50mg caplets) 50-count bottles, Manufactu
Recalled February 9, 2022 · FDA recall D-0470-2022 · Ultra Seal
Hazard
cGMP deviations · FDA Class II
Units
174,852 bottles
Sold at
Nationwide within the United States
Description
cGMP deviations
Product
Legatrin PM Pain Reliever/Sleep Aid (acetaminophen 500 mg, diphenhydramine HCl 50mg caplets) 50-count bottles, Manufactured for: Church & Dwight Co., Inc. Ewing, NJ 08628 NDC 10237-907-50
Manufacturer(s)
Ultra Seal Corporation
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →