Pepsin 1:3000 Powder, 50 kg, Item #FTI-G0193-00, American Laboratories 5036 South 33rd Street, Omaha, Nebraska 68107. Pa
Summary
The FDA issued a Class II for Pepsin 1:3000 Powder, 50 kg, Item #FTI-G0193-00, American Laboratories 5036 Sout by American Laboratories, LLC. Reason: Potential Salmonella contamination..
Details
Source
Food Recall
External ID
H-0612-2026
Action Date
2026-04-01
Status
Terminated
Category
food
Product Description
Pepsin 1:3000 Powder, 50 kg, Item #FTI-G0193-00, American Laboratories 5036 South 33rd Street, Omaha, Nebraska 68107. Packed in double poly-lined cardboard drums or boxes.
Lot/Code Info: Manufacturing code: 001 Lot Code: 00160041 Reevaluation date: February 2, 2029
Quantity Affected: 468 kg
Reason for Recall
Potential Salmonella contamination.
Distribution
11 direct wholesale accounts located in AZ, CA, FL, MO, NM, OH, SC, UT, WI. 1 direct wholesale account located in Australia.
Type: Voluntary: Firm initiated
Recall Initiated: 2026-02-26
Company
Omaha, NE
Context & Analysis
This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.
This was one of 64 food recalls issued in the same week, part of 204 food-related FDA actions this month.
American Laboratories, LLC has 3 FDA actions in our database, including 3 recalls.
Frequently Asked Questions
What is a Class II recall?
A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (American Laboratories, LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does American Laboratories, LLC have FDA actions?
American Laboratories, LLC has 3 FDA actions in our database, including 3 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "H-0612-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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