Class IITerminated in FDA datasetRecall initiated Feb 26, 2026

Pepsin Full Strength Powder, 50 kg, Item #5000545, American Laboratories 5036 South 33rd…

Recalling firm: American Laboratories, LLC

Why it was recalled

Potential Salmonella contamination.

Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: May 8, 2026.

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ProductPepsin Full Strength Powder, 50 kg, Item #5000545, American Laboratories 5036 South 33rd Street, Omaha, Nebraska 68107. Packed in double poly-lined cardboard drums or boxes.
Package size50 kg

FDA code information

Manufacturing code: 294 Lot Code: 29460025 Reevaluation date: January 20, 2029

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Full FDA record and distribution details

Original product description

Pepsin Full Strength Powder, 50 kg, Item #5000545, American Laboratories 5036 South 33rd Street, Omaha, Nebraska 68107. Packed in double poly-lined cardboard drums or boxes.

Extracted codes and context

TypeCode / valueContext
lot29460025Manufacturing code: 294 Lot Code: 29460025 Reevaluation date: January 20, 2029

Original FDA recall reason

Potential Salmonella contamination.

Recall details

Recall number
H-0610-2026
Event ID
98497
FDA status
Terminated
Initiated
Feb 26, 2026
Reported
Apr 1, 2026
Classified
Mar 20, 2026
Terminated
May 8, 2026
Quantity
400 kg
Location
Omaha, NE, United States
Initiation type
Voluntary: Firm initiated
Notification
E-Mail

Where it was distributed

11 direct wholesale accounts located in AZ, CA, FL, MO, NM, OH, SC, UT, WI. 1 direct wholesale account located in Australia.

FDA source record · H-0610-2026

Data updated September 16, 2026. View official FDA data ↗

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