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Class II: temporary or reversible health riskTerminated

AMPI Whey Powder Recall

AMPI Whey Powder, Sweet Type, Formula 521, Extra Grade, spray process pasteurized, pack…

AMPI · New Ulm, MN

Risk level
Class II
Reported by FDA
Aug 1, 2018
Recall ID
F-1773-2018
Check your lot numberHow we source this data

Summary

Ampi recalled AMPI Whey Powder starting Jul 16, 2018. The FDA classified it as Class II (temporary or reversible health risk) and published enforcement report F-1773-2018 on Aug 1, 2018. Reason: Whey powder may have the potential to be contaminated with Salmonella. Status: Terminated.

Why it was recalled

Whey powder may have the potential to be contaminated with Salmonella.

Product description

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).

Lot numbers, UPCs & expiration codes

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

GA, IL, KY, MI, MN, MO, OH, PA, VA

What to do if you have this product

  • Compare the brand, size, and lot/UPC codes on your package with the codes above.
  • If it matches, don't eat it. Return it to the store for a refund or throw it away.
  • Wash surfaces and containers that touched the product.
  • If you feel sick after eating it, contact your doctor. In an emergency call 911.

Recall details

Recall number
F-1773-2018
Classification
Class II
Status
Terminated
Recall initiated
Jul 16, 2018
FDA report date
Aug 1, 2018
Quantity
1,783,715.81 lbs.
Recall type
Voluntary: Firm initiated
Recalling firm
AMPI

Original FDA data

Every field from FDA enforcement report F-1773-2018, exactly as published.

Show all FDA fields
City
New Ulm
State
MN
Status
Terminated
Country
United States
Event ID
80537
Address
315 N Broadway St
Code information
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
Postal code
56073-1719
Report date
Aug 1, 2018
Product type
Food
Recall number
F-1773-2018
Classification
Class II
Recalling firm
AMPI
Product quantity
1,783,715.81 lbs.
Termination date
Apr 5, 2024
Reason for recall
Whey powder may have the potential to be contaminated with Salmonella.
Voluntary / mandated
Voluntary: Firm initiated
Product description
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).
Distribution pattern
GA, IL, KY, MI, MN, MO, OH, PA, VA
Recall initiation date
Jul 16, 2018
Initial firm notification
Letter
Center classification date
Aug 13, 2018

How we source this data

Source: U.S. Food and Drug Administration enforcement report F-1773-2018, published Aug 1, 2018. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: . Content last changed: .

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