Quick Facts at a Glance
- Recall Date
- February 26, 2026
- Hazard Level
- HIGH
- Brand
- American Laboratories
- Category
- Food & Beverages
- Sold At
- Multiple Retailers
- Geographic Scope
- 9 states
- At-Risk Groups
- GENERAL
What to Do Now
Use this page like a recall checklist: verify the product first, then act on the official remedy.
Immediate steps
- 1Stop using the product until you confirm whether it is included in the recall.
- 2Compare the product label, model number, UPC, color, size, and purchase location against the identifiers below.
- 3Follow the official remedy from FDA - Food Safety; save photos, receipts, labels, and correspondence before contacting the company.
- 4If the product could harm a child, older adult, pet, or patient, move it out of reach immediately.
Check these identifiers
- Brand
- American Laboratories
- Product type
- Pepsin Powder
- Model numbers
- Manufacturing code: 294 Lot Code: 29460025 Reevaluation date: January 20, 2029
- Sold at
- Multiple Retailers
- Where affected
- AZ, CA, FL, MO, NM, OH, SC, UT +1 more
Recall Timeline
Key dates and source checks for this recall record.
Recall announced
February 26, 2026
Reported by FDA FOOD
April 1, 2026
RecallRadar source check
April 8, 2026
Consumer action
Use the official remedy and keep documentation.
Hazard Information
Potential Salmonella contamination.
What You Should Do
Consumers who have purchased this product should not consume it. Contact American Laboratories, LLC for refund or replacement information. Notification method: E-Mail
About This Product
Pepsin Full Strength Powder is a digestive enzyme product sold in bulk form for use in manufacturing or as an ingredient. It is packaged in double poly-lined drums or boxes.
Why This Is Dangerous
Salmonella contamination can cause foodborne illness in humans. Contaminated enzyme powder can enter food-processing workflows or end-use products.
Industry Context
This recall is not part of a broader industry pattern.
Real-World Impact
The recall may disrupt supply for manufacturers relying on this ingredient and pose a clear health risk to consumers if unknowingly used.
Practical Guidance
How to identify if yours is affected
- Check Item #5000545 on packaging.
- Verify batch identifiers: Manufacturing code 294 and Lot Code 29460025.
- Note Reevaluation date: January 20 and any reference to 2029.
Where to find product info
Recall notice and FDA enforcement page linked in the official recall communication. Packaging labels should show the item number and codes.
What timeline to expect
Refunds or replacements typically take 4-8 weeks.
If the manufacturer is unresponsive
- Escalate to FDA recall program or consumer protection agency
- Document all communication attempts and responses
- Consider legal counsel if no resolution after a reasonable period.
How to prevent similar issues
- Request Certificates of Analysis from suppliers
- Verify batch traceability for future purchases
- Audit GMP controls and recall readiness with suppliers
- Keep updated recall contacts and monitor FDA recall listings
Documentation advice
Retain recall notices, purchase records, batch/lot codes, correspondence with the supplier, and any medical records if illness occurs.
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Product Details
Item number: 5000545. Sold through 11 direct wholesale accounts in AZ, CA, FL, MO, NM, OH, SC, UT, WI and 1 account in Australia. Packaging: double poly-lined cardboard drums or boxes. Quantity: 400 kg. Recall date: 2026-02-26. Status: Active. Price: Unknown.
Reported Incidents
No injuries or incidents have been reported.
Key Facts
- Direct wholesale accounts in 11 U.S. states and Australia
- Salmonella contamination risk
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Safety Guide
Not sure what to do next? Our guide walks you through the process step by step.
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