FDA recall record

American Laboratories Pepsin 1:10,000 Powder, 10 kg, Item #FTI-G0193-00, American recall — FDA H-0611-2026

Potential Salmonella contamination.

Class IIclassification
H-0611-2026official record ID
Apr 1, 2026report date

Recall record at a glance

Official recordH-0611-2026
CategoryFood Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmAmerican Laboratories, LLC
Report dateApr 1, 2026
Recall initiation dateFeb 26, 2026
Quantity370 kg
LocationOmaha, NE, United States

Official product description

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.

Why the product was recalled

Potential Salmonella contamination.

Distribution information

11 direct wholesale accounts located in AZ, CA, FL, MO, NM, OH, SC, UT, WI. 1 direct wholesale account located in Australia.

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: E-Mail.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

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