American Laboratories, LLC is recalling 1,238 units of Pepsin Full Strength, 1:10,000, and 1:3000 powders due to potential Salmonella contamination. These products were distributed to 11 wholesale accounts across several U.S. states and one account in Australia. Consumers and businesses should check their inventory for these specific enzyme powders packed in cardboard drums or boxes.
Salmonella is a pathogen that can cause serious and sometimes fatal infections, particularly in young children, frail or elderly people, and others with weakened immune systems. Healthy individuals often experience fever, diarrhea, nausea, vomiting, and abdominal pain.
You have 2 options:
Manufacturing code: 294; Reevaluation date: January 20, 2029; Packed in double poly-lined cardboard drums or boxes.
Manufacturing code: 005; Reevaluation date: January 19, 2029; Packed in double poly-lined cardboard drums or boxes.
Manufacturing code: 001; Reevaluation date: February 2, 2029; Packed in double poly-lined cardboard drums or boxes.
If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.
This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.
AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.
Sources: FDA iRES · Raw API Response
openFDA Disclaimer: This recall information is sourced from the openFDA API. 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. Refer to the openFDA terms of service for more information.