This recall is archived. It was completed or terminated more than 90 days ago.
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American Laboratories: 3 products
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FOOD RECALLMODERATE

American Laboratories: 3 products

American Laboratories recalls pepsin powders (Full Strength, 1:10,000, 1:3000) due to potential Salmonella contamination.

What to do

Consumers who purchased any of the recalled pepsin powder products should stop using them immediately and contact American Laboratories, LLC for a refund or replacement. Do not consume or use the product if you have it.

Recalled
Listed
Updated
Recall No.
H-0612-2026
Agency
FDA
Firm
American Laboratories, LLC
Recall ID
98497
Status
TERMINATED

Why it was recalled

American Laboratories, LLC is recalling multiple pepsin powder products due to potential Salmonella contamination. The affected products include Pepsin Full Strength Powder, 50 kg, Item #5000545; Pepsin 1:10,000 Powder, 10 kg, Item #FTI-G0193-00; and Pepsin 1:3000 Powder, 50 kg, Item #FTI-G0193-00. The products were packed in double poly-lined cardboard drums or boxes.

Is mine affected?

Check the lot code and best-by (or expiration) date printed on your package. Yours is affected if it matches one below.

ProductUPCRecall #
Pepsin 1:3000 Powder, 50 kg, Item #FTI-G0193-00, American Laboratories 5036 South 33rd Street, Omaha, Nebraska 68107. Packed in double poly-lined cardboard drums or boxes.00160041H-0612-2026
Pepsin Full Strength Powder, 50 kg, Item #5000545, American Laboratories 5036 South 33rd Street, Omaha, Nebraska 68107. Packed in double poly-lined cardboard drums or boxes.29460025H-0610-2026
Pepsin 1:10,000 Powder, 10 kg, Item #FTI-G0193-00, American Laboratories 5036 South 33rd Street, Omaha, Nebraska 68107. Packed in double poly-lined cardboard drums or boxes.00560021H-0611-2026

Where it was sold

Distributed in Arizona, California, Florida, Missouri, New Mexico, Ohio, South Carolina, Utah, and Wisconsin.

Timeline

  1. Firm initiated recall
  2. Publicly announced
  3. Listed on Recall Canary
  4. Recall ended
  5. Archived
  6. Summary updated
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Editorial summary by Recall Canary · summary updated 2026-08-20 · primary source: U.S. Food and Drug Administration · severity reflects the agency's published classification