FDA recall record
AMPI Whey Powder, Sweet Type, Formula 521, Extra Grade, spray process pasteurized, packaged in 50 lbs net (22.68 kg net) and 25 kg net (55.12 lbs net).
FDA classification. FDA Class I, II, and III are not the same as USDA FSIS classifications and are not a cross-agency safety score.
FDA listed a termination date of April 5, 2024. openFDA does not treat this as a live recall-status tracker.
Product described in an FDA recall
AMPI Whey Powder, Sweet Type, Formula 521, Extra Grade, spray process pasteurized, packaged in 50 lbs net (22.68 kg net) and 25 kg net (55.12 lbs net).
Reason
Whey powder may have the potential to be contaminated with Salmonella.
Products involved
Product descriptions are copied from the FDA recall record. They are not a current catalog and are not automatically matched to WhoMadeMyFood product pages.
AMPI Whey Powder, Sweet Type, Formula 521, Extra Grade, spray process pasteurized, packaged in 50 lbs net (22.68 kg net) and 25 kg net (55.12 lbs net).
Code information listed by FDA
Lot Serial Number: 7000.118.121.BL - 7000.118.125.BL, 7000.118.144.BL - 7000.118.149.BL, 7000.118.153.BL - 7000.118.156.BL, 7000.118.158.BL - 7000.118.165.BL
Distribution and firm information
Recalling firm listed by FDA: AMPI
Firm location listed by FDA: New Ulm, MN, United States
Distribution reported by FDA: GA, IL, KY, MI, MN, MO, OH, PA, VA
Product quantity listed by FDA: 1,783,715.81 lbs.
Source
Source: U.S. Food and Drug Administration (FDA), openFDA food enforcement reports.
Official FDA openFDA food enforcement record
Identifying an FDA recall record does not imply FDA endorsement of WhoMadeMyFood. Methodology.