FDA recall H-0610-2026 · Apr 1, 2026
American Laboratories, LLC: Pepsin Full Strength Powder recall
Product
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.
Reason for recall
Potential Salmonella contamination.
What to do
FDA enforcement reports don't include consumer instructions. Check the codes below against your package, and look for the company's notice on FDA's recalls page. If you have the product and aren't sure, don't use it until you've checked.
Recall details
- FDA classification
- Class II: use of or exposure to the product may cause temporary or medically reversible health problems, or the chance of serious problems is remote.
- Status
- Terminated
- Codes, lots and dates
- Manufacturing code: 294 Lot Code: 29460025 Reevaluation date: January 20, 2029
- Quantity
- 400 kg
- Distribution
- 11 direct wholesale accounts located in AZ, CA, FL, MO, NM, OH, SC, UT, WI. 1 direct wholesale account located in Australia.
- Recalling firm
- American Laboratories, LLC, Omaha, NE
- Voluntary or mandated
- Voluntary: Firm initiated
- Recall started
- 2026-02-26
Source: openFDA enforcement record H-0610-2026 · search recall number H-0610-2026 in FDA's Enforcement Report.
Copied from the agency record without changes. Data as of Oct 14, 2026, 1:15 AM EDT. The agency notice is the final word.
Check something else