AMPI Buttermilk Powder
Reason The Buttermik powder may contain a Foreign Material (metal).
AMPI Whey Powder recall
Recalled by Ampi · New Ulm, MN, United States
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Why it was recalled
Whey powder may have the potential to be contaminated with Salmonella.
Pathogen: Salmonella
Salmonella is the most common cause of food recalls for bacteria, often in eggs, produce, nuts and spices.
The most serious food recalls: a contaminated product can cause outbreaks, hospitalisations and deaths, especially for pregnant people, young children, older adults and anyone with a weakened immune system. All bacteria & viruses recalls.
What was recalled
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).
Quantity: 1,783,715.81 lbs.
Lot codes, dates and UPCs
A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.
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
Where it was sold
Georgia Illinois Kentucky Michigan Minnesota Missouri Ohio Pennsylvania Virginia
FDA's distribution note: GA, IL, KY, MI, MN, MO, OH, PA, VA
Check the codes, then return or discard. Class II means eating it may cause temporary or reversible health problems. If your package matches the recalled codes, do not eat it - return it to the store or throw it away. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.
- Recalling firm
- Ampi
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Jul 16, 2018
- In FDA report of
- Aug 1, 2018
- Terminated
- Apr 5, 2024
- FDA recall number
- F-1773-2018 · event 80537
- Official record
- FDA enforcement report search