Pepsin 1:10,000 Powder, 10 kg, Item #FTI-G0193-00
Recalled by American Laboratories, LLC
Food recall
American Laboratories, LLC
Class II — moderate
Using this product might cause a temporary or medically reversible health problem. The chance of serious harm is low.
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.
Who this recall affects
This recall matters most to young children, adults over 65, pregnant people, and anyone with a weakened immune system. Public health authorities note these groups are more likely to develop a severe Salmonella infection rather than a short-lived stomach illness.
Distribution listed in the notice: 11 direct wholesale accounts located in AZ, CA, FL, MO, NM, OH, SC, UT, WI. 1 direct wholesale account located in Australia..
What Salmonella actually means
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.
In this case, the concern applies specifically to Pepsin 1:10,000 Powder, 10 kg, Item #FTI-G0193-00 from American Laboratories, LLC — not to the wider category of products. Similar items from other brands aren't part of this recall.
How to check whether you have it
On packaged food, lot codes and best-by dates are usually printed in small date-coding ink on the side seam, the bottom of the package, or near the top seal — not on the front label. The UPC barcode is on the back or bottom.
Compare what you find against the identifying details in this recall: Manufacturing code: 005 Lot Code: 00560021 Reevaluation date: January 19, 2029
What to do if you already bought it
Do not eat the product, even if it looks and smells normal — contamination is usually invisible.
Return it to the store for a refund, or throw it away in a sealed bag so pets and wildlife can't reach it.
If it touched other food or surfaces, wash those surfaces and your hands with hot soapy water. When in doubt, contact American Laboratories, LLC or your local health department.
Full recall details
- Status
- Terminated
- Date reported
- April 1, 2026
- Recall started
- February 26, 2026
- Distributed in
- NE
What you can do
Check whether any product you have matches the description and codes above. If it does, stop using it and follow the instructions in the official recall notice. When in doubt, contact the company or your local health authority.
Quick answers
Why was Pepsin 1:10,000 Powder, 10 kg, Item #FTI-G0193-00 recalled?+
According to the FDA: Potential Salmonella contamination.
How serious is this recall?+
Class II — moderate. Using this product might cause a temporary or medically reversible health problem. The chance of serious harm is low.
What should I do if I have Pepsin 1:10,000 Powder, 10 kg, Item #FTI-G0193-00?+
Compare your product against the description and identifying codes on this page. If it matches, stop using it and follow the instructions in the official recall notice — this usually means returning it for a refund or discarding it. When in doubt, contact the company or your local health authority.
Opens the U.S. Food and Drug Administration (FDA) data for this recall.
Recall number: H-0611-2026. Information last synced from the FDA on October 9, 2026.
