Class IITerminated in FDA datasetRecall initiated Feb 26, 2026

Pepsin 1:10,000 Powder, 10 kg, Item #FTI-G0193-00, 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 1:10,000 Powder, 10 kg, Item #FTI-G0193-00, American Laboratories 5036 South 33rd Street, Omaha, Nebraska 68107. Packed in double poly-lined cardboard drums or boxes.
Package size10 kg

FDA code information

Manufacturing code: 005 Lot Code: 00560021 Reevaluation date: January 19, 2029

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Full FDA record and distribution details

Original product description

Pepsin 1:10,000 Powder, 10 kg, Item #FTI-G0193-00, American Laboratories 5036 South 33rd Street, Omaha, Nebraska 68107. Packed in double poly-lined cardboard drums or boxes.

Extracted codes and context

TypeCode / valueContext
lot00560021Manufacturing code: 005 Lot Code: 00560021 Reevaluation date: January 19, 2029

Original FDA recall reason

Potential Salmonella contamination.

Recall details

Recall number
H-0611-2026
Event ID
98497
FDA status
Terminated
Initiated
Feb 26, 2026
Reported
Apr 1, 2026
Classified
Mar 20, 2026
Terminated
May 8, 2026
Quantity
370 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-0611-2026

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

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