Class IITerminatedVoluntary: Firm initiated
American Laboratories, LLC: food recall H-0612-2026
American Laboratories, LLC of Omaha, NE recalled Pepsin 1:3000 Powder, 50 kg, Item #FTI-G0193-00, American Laboratories 5036 South 33rd Street, Omaha, Nebraska 68107.… Reason: Potential Salmonella contamination. The FDA listed it as Class II in its Enforcement Report dated Apr 1, 2026; distribution: Arizona, California, Florida, Missouri, New Mexico, Ohio, South Carolina, Utah, Wisconsin.
Record status as published: Terminated (terminated May 8, 2026). openFDA data last updated Oct 21, 2026.
Have this product? Check FDA.gov and your retailer. This page reproduces an FDA Enforcement Report record and is not a public alert. Look for the firm's recall notice on the FDA's recalls page, or ask the store where you bought it what to do. If you think you got sick from a food, contact a health care provider.
Recall details
- Product
- 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.
- Product quantity
- 468 kg
- Reason for recall
- Potential Salmonella contamination.
- Codes, lots and dates on the package
- Manufacturing code: 001 Lot Code: 00160041 Reevaluation date: February 2, 2029
- Distribution pattern
- 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
- Classification
- Class II — the FDA uses this class for a situation in which using or being exposed to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
- Voluntary or mandated
- Voluntary: Firm initiated
- How the firm first notified customers
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Dates
| Event | Date |
|---|---|
| Recall initiated by the firm | Feb 26, 2026 |
| Classified by the FDA | Mar 20, 2026 |
| Published in the Enforcement Report | Apr 1, 2026 |
| Terminated | May 8, 2026 |
Other products in the same recall event
The FDA groups related products under one recall event (event 98497).
- H-0611-2026 — 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.
- H-0610-2026 — 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.
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Sources
- U.S. Food and Drug Administration, openFDA food enforcement reports, recall number H-0612-2026 (openFDA record). Data provided by the U.S. Food and Drug Administration (https://open.fda.gov).
- Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service. The FDA does not endorse OpenPlate.