Pepsin Full Strength Powder recall
Recalled by American Laboratories, LLC
The product, as the FDA describes it: 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.
Why it was recalled
Potential Salmonella contamination.
The FDA has since closed this recall out, which means the company finished removing the product from sale. It is kept here because a closed recall still matters to anyone holding a package bought before it ended.
What to do if you have it
Nothing about pepsin full strength powder will look or smell wrong, because the organisms behind this kind of recall leave no trace you can see or taste. Do not cook it to make it safe and do not sample it. Throw it out or return it, then wash anything it touched, including the shelf it sat on and the container beside it.
How to tell whether your package is one of them
A recall covers particular production runs, not everything the company makes, so the codes decide it. These are the ones the FDA published. Match them against what is printed on your package, usually near the best-before date.
Manufacturing code: 294 Lot Code: 29460025 Reevaluation date: January 20, 2029
The details on record
| Recalling company | American Laboratories, LLC |
|---|---|
| Company location | Omaha, NE |
| Where it was distributed | 11 direct wholesale accounts located in AZ, CA, FL, MO, NM, OH, SC, UT, WI. 1 direct wholesale account located in Australia. |
| How much was recalled | 400 kg |
| Recall started | February 26, 2026 |
| Published by the FDA | April 1, 2026 |
| Recall type | Voluntary: Firm initiated |
| How the company announced it | |
| FDA recall number | H-0610-2026 |
Everything above comes from the FDA enforcement report for this recall. Read the official notice for the company's own wording, contact numbers, and any photographs of the packaging.
The other half of the answer
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