Ultra Seal Corporation recalls FEM-PRIN MENSTRUAL RELIEF (acetaminophen 325 mg, pamabrom 25mg) tablets, 2-count packets, Manufactured for: HARTHealth S
Recalled February 9, 2022 · FDA recall D-0509-2022 · Ultra Seal
Hazard
cGMP deviations · FDA Class II
Units
223,090 packets
Sold at
Nationwide within the United States
Description
cGMP deviations
Product
FEM-PRIN MENSTRUAL RELIEF (acetaminophen 325 mg, pamabrom 25mg) tablets, 2-count packets, Manufactured for: HARTHealth Seattle, WA 98124
Manufacturer(s)
Ultra Seal Corporation
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →