Pepsin 1:10,000 Powder, 10 kg, Item #FTI-G0193-00

American Laboratories, LLC has recalled Pepsin 1:10,000 Powder, 10 kg, Item #FTI-G0193-00, according to data published by the U.S. Food and Drug Administration (FDA). The recall was reported on April 1, 2026 and was initiated on February 26, 2026. It is classified as a Class II recall, which means using this product might cause a temporary or medically reversible health problem. The chance of serious harm is low.

Below is a plain-English summary of what was recalled, why it was recalled, how to tell whether you have the affected product, and what steps you can take. For the complete and most current details, you can view the FDA record linked further down this page.

What was recalled?

This recall covers Pepsin 1:10,000 Powder, 10 kg, Item #FTI-G0193-00, with approximately 370 kg affected. The company behind the recall is American Laboratories, LLC, based in Omaha, NE. The FDA describes the product as: “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 was Pepsin 1:10,000 Powder, 10 kg, Item #FTI-G0193-00 recalled?

According to the FDA, the stated reason for the recall is: “Potential Salmonella contamination.” In plain terms, this recall relates to Salmonella.

Salmonella is a group of bacteria that is one of the most common causes of foodborne illness in the United States. Public health authorities note that infections can lead to symptoms such as fever, diarrhea, and stomach cramps, and that young children, older adults, and people with weakened immune systems are at higher risk of serious illness. Because it can spread through contaminated food, regulators treat Salmonella findings seriously.

What should you do?

If you think you may have bought Pepsin 1:10,000 Powder, 10 kg, Item #FTI-G0193-00, compare it against the product description and identifying codes (Manufacturing code: 005 Lot Code: 00560021 Reevaluation date: January 19, 2029) before using it.

The general guidance for a matching product is to stop using it and follow the instructions in the official FDA recall notice, which may include a repair, replacement, refund, or safe disposal. When in doubt, contact American Laboratories, LLC or your local health authority.

About this recall

This recall was distributed in NE. RecallRadar summarizes recall information from public FDA data to make it easier to understand. We are an independent service and are not affiliated with the FDA or any government agency, so please always refer to the official source for the authoritative record — and note the “last synced” date shown on this page, since recall details can change over time.