← FDA ENFORCEMENT
H-0610-2026Class II

American Laboratories, LLC

Recalling firm
American Laboratories, LLC
Product type
Food / supplement / cosmetic
Status
Terminated
Report date
2026-04-01
Distribution
11 direct wholesale accounts located in AZ, CA, FL, MO, NM, OH, SC, UT, WI. 1 direct wholesale account located in Australia.
Firm state
NE
Product quantity
400 kg
Initiated by
Voluntary: Firm initiated
SPEQ quality domain
Environmental Monitoring
Reason for recall

Potential Salmonella contamination.

Product description

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.

Code / lot info

Manufacturing code: 294 Lot Code: 29460025 Reevaluation date: January 20, 2029

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Data: U.S. FDA openFDA enforcement API. Recall details are as reported by the FDA. The quality-domain mapping and severity are a SPEQ editorial interpretation of the recall reason, not an official FDA classification.