Malt Products Corporation recalls Diastatic Malt Powder 50lb bags with potential Salmonella contamination. Affected lots include 21L14 and 21L15, expiring June 2022. Consumers should check product details to determine if affected.
“Malt Products Corporation Diastatic Malt Powder Recall: Salmonella Contamination Risk.” GovInfoNow, updated October 4, 2026. https://govinfonow.com/recall/13336-malt-products-corporation-diastatic-malt-powder-recall-salmonella-contamination-risk. Based on FDA recall #F-0801-2022 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0801-2022%22&limit=1).
The FDA announced on Feb. 11, 2022, that Malt Products Corporation voluntarily recalled Diastatic Malt Powder due to potential Salmonella contamination. Owners should contact the company for a refund.
How to tell if you have it
Brand: Malt Products Corporation
Product: Diastatic Malt Powder 50lb bag
Lot Numbers: 21L14, 21L15
Product Numbers: 89DP
Expiration Dates: 06/14/22, 06/15/22
Distribution states: AZ, CA, CT, FL, IL, MA, MD, MI, ND, NJ, NY, OH, PA, RI
The hazard
The product poses a potential contamination risk with Salmonella. The FDA classified the recall as Class II.
Context
GovInfoNow's records show other recent recalls of similar products include California Dairies Low Heat Non-Fat Dried Milk Powder Recall (2026-04-20), American Laboratories Pepsin Powder Recall (2026-02-26), and Bulk & Organic Moringa Powder Recall (2025-10-31).
How to tell if you have this one
Check for lot numbers 21L14 or 21L15 on the packaging. The product expires by June 14 or 15, 2022, and comes in 50lb bags per pallet.
Brand
Malt Products Corporation
Category
Food
Based on the official FDA remedy
What to do — step by step
Check Product Details
Look for lot numbers 21L14 or 21L15 on the packaging to confirm if the product is affected.
Where it went and when
Where it was distributed
Distributed in 14 states.
Listed by the agency
Not listed
FDA distribution: “AZ, CA, CT, FL, IL, MA, MD, MI, ND, NJ, NY, OH, PA, RI” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Arizona, California, Connecticut, Florida, Illinois, Maryland, Massachusetts, Michigan, New Jersey, New York, North Dakota, Ohio, Pennsylvania, Rhode Island.
Recall timeline
FDA terminated this recall 47 days after the firm started it.
1Firm started the recall
2FDA classified it Class II
3Published in FDA’s Enforcement Report
4FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
Official source: FDA Recall #F-0801-2022 (February 11, 2022) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0801-2022 to see it in context.
Plain-language summary written by qwen3:4b on October 4, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.