Ultra Seal Corporation recalls Backache & Muscle Relief (acetaminophen 250 mg, magnesium salicylate-tetrahydrate 290mg, caffeine 50 mg) 2 tablets per p
Recalled February 9, 2022 · FDA recall D-0482-2022 · Ultra Seal
Hazard
cGMP deviations · FDA Class II
Units
5,107,565 packets
Sold at
Nationwide within the United States
Description
cGMP deviations
Product
Backache & Muscle Relief (acetaminophen 250 mg, magnesium salicylate-tetrahydrate 290mg, caffeine 50 mg) 2 tablets per packet, Mfd. for First Aid Direct, Mason, OH 45040, NDC 42961-111-832
Manufacturer(s)
Ultra Seal Corporation
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →