American Laboratories recalls 10kg Pepsin 1:10,000 Powder (Item #FTI-G0193-00) due to potential Salmonella contamination. Consumers should check product details and follow official recall instructions.
Potential Salmonella contamination.
American Laboratories is recalling 10kg Pepsin 1:10,000 Powder (Item #FTI-G0193-00) because it may contain Salmonella bacteria. This poses a risk of foodborne illness if the product is used in food preparation.
Salmonella bacteria can cause foodborne illness, including symptoms like diarrhea, fever, and abdominal cramps. The contamination may occur during manufacturing or handling of the product.
Anyone who owns or uses this specific Pepsin powder for food processing or laboratory work. Those handling the product in food preparation are at slightly higher risk.
Check for the product name 'Pepsin 1:10,000 Powder', 10 kg size, and item number #FTI-G0193-00. The manufacturing code is 005 and lot code 00560021.
Look for the product name 'Pepsin 1:10,000 Powder', 10 kg size, and item number #FTI-G0193-00 on the packaging.
The recall states there is potential Salmonella contamination, so it is not safe to use without following the recall instructions.
Check for the product name 'Pepsin 1:10,000 Powder', 10 kg size, and item number #FTI-G0193-00 on the packaging. The manufacturing code is 005 and lot code 00560021.
The recall does not specify a remedy, so contact American Laboratories for further instructions.
We’ve drafted a message you can send American Laboratories to request your refund or repair — edit it as you like.
Subject: Recall H-0611-2026 — American Laboratories American Laboratories Hello, I own a American Laboratories that is covered by recall H-0611-2026 from American Laboratories. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
