HIGH

American Laboratories Pepsin Full Strength Powder Recalled for Salmonella Contamination (400 kg, 202

American Laboratories recalled 400 kg of Pepsin Full Strength Powder sold to 11 direct wholesale accounts in AZ, CA, FL, MO, NM, OH, SC, UT, WI and one wholesale account in Australia after a recall cited potential Salmonella contamination. The product is Item #5000545 and packed in double poly-lined drums or boxes. Consumers should not consume this product and should contact American Laboratories,

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

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

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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

  1. Check Item #5000545 on packaging.
  2. Verify batch identifiers: Manufacturing code 294 and Lot Code 29460025.
  3. 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.

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

  • 400 kg recalled
  • Item #5000545
  • Direct wholesale accounts in 11 U.S. states and Australia
  • Salmonella contamination risk
  • Recall date 2026-02-26
  • Active recall

Safety Guide

Not sure what to do next? Our guide walks you through the process step by step.

Read: What to Do When You Find a Recalled Product

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Safety Assessment

Risk LevelHIGH
Severity Score
8/ 10
Affected Groups
GENERAL
Injury Types
POISONING

Product Details

Model Numbers
Manufacturing code: 294 Lot Code: 29460025 Reevaluation date: January 20
2029
Affected States
AZ, CA, FL, MO, NM, OH, SC, UT, WI
Report Date
April 1, 2026
Source Agency
FDA - Food Safety
Recall Status
ACTIVE

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