PlainRecalls
ModerateClass IITerminated

FDA Food recall · Reported April 1, 2026

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.

Potential Salmonella contamination.

Recall #
H-0611-2026
Affected scope
370 kg
Initiated
February 26, 2026
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The recall

American Laboratories, LLC issued this moderate-severity FDA Food recall — Potential Salmonella contamination..

Moderate
severity level
Class II
classification
April 1, 2026
reported

Sourced from official FDA Food enforcement records. Verify recall #H-0611-2026 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.

Recall Insight

This FDA Food action (record #H-0611-2026) was formally reported on April 1, 2026, with the manufacturer initiating the action on February 26, 2026. It is classified under Moderate severity (Class II), with a current status of Terminated. American Laboratories, LLC is listed as the recalling firm, operating out of Omaha, NE. Federal records list the affected scope as 370 kg.

The documented reason for this recall is: Potential Salmonella contamination. Distribution data in the federal record shows the product reached: 11 direct wholesale accounts located in AZ, CA, FL, MO, NM, OH, SC, UT, WI. 1 direct wholesale account located in Australia.. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.

Within the same product category the archive holds 6 closely related recalls, 2 from FDA Food — clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.

Vehicles recalls over time

Where this recall sits in its category — 9,301 vehicles recalls on record

02004006008001,000 20052008201120142017202020232026 109

Where this recall sits in the database

Severity2366872097High severity (most serious)Moderate severityLow severity
Where this recall sits in the database

Of 100,165 recalls in the database, 23,668 are high severity, 72,097 moderate, and 4,400 low. This recall is classified moderate severity.

Severity

Moderate

Affected scope

370 kg

Related Recalls

6

2 from same agency

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.

Reason for recall

Potential Salmonella contamination.

Recall Profile

Structured summary of the FDA Food recall record
Attribute Value
Agency U.S. Food and Drug Administration
Severity class Moderate (Class II)
Status Terminated
Recall number H-0611-2026
Date reported April 1, 2026
Date initiated February 26, 2026
Recalling firm American Laboratories, LLC
Firm location Omaha, NE
Affected scope 370 kg
Distribution 11 direct wholesale accounts located in AZ, CA, FL, MO, NM, OH, SC, UT, WI. 1 direct wholesale account located in Australia.

Profile values are sourced directly from the official FDA Food enforcement record. Source: U.S. Food and Drug Administration.

What to do with this recall

Match your product against the recall record, then act on the agency remedy.

  • Check the recall number (H-0611-2026) and product description against the item you own. Search the archive
  • Confirm the current status with FDA Food before acting — recall details can be updated.
  • Follow the documented remedy (refund, replacement, repair, or disposal) rather than general advice. What to do next

This page summarizes the official FDA Food record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.

Frequently Asked Questions

What product was recalled?
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.. Recalled by American Laboratories, LLC. Units affected: 370 kg.
Why was this product recalled?
Potential Salmonella contamination.
Which agency issued this recall?
This recall was issued by the FDA Food on April 1, 2026. Severity: Moderate. Recall number: H-0611-2026.
Where was the recalled product distributed?
Distribution: 11 direct wholesale accounts located in AZ, CA, FL, MO, NM, OH, SC, UT, WI. 1 direct wholesale account located in Australia..
How do I check if my product is affected by a recall?
Check the product description and recall number (H-0611-2026) against your product. Visit the official FDA Food website for the most current information. You can also use our Recall Checker tool to search by product name or brand.
What are the health risks of consuming a recalled food product?
Recalled food products may contain contaminants, undeclared allergens, or harmful bacteria such as Salmonella, Listeria, or E. coli. Consuming these products can cause foodborne illness ranging from mild gastrointestinal symptoms to serious conditions requiring hospitalization. If you have consumed a recalled food product and experience symptoms, contact your healthcare provider and report to the FDA via MedWatch.

Nearby Recalls in This Category

Other recalls in the same product category — useful for spotting patterns across the same defect class or manufacturer.

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Data Sources

Source: FDA, CPSC, and NHTSA federal recall databases. This recall: FDA Food, reported April 1, 2026.

  • Source: FDA — Food and Drug Administration, openFDA Enforcement API (food, drug, and medical device recalls)
  • Source: CPSC — Consumer Product Safety Commission Recalls API (consumer product recalls and hazards)
  • Source: NHTSA — National Highway Traffic Safety Administration Recalls API (vehicle safety recalls)

Recall information is sourced from official federal agency databases. Always verify recall details with the issuing agency for the most current status. This information is for research and awareness purposes only.

Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records — no number is typed in by an editor. Severity classes follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type), and related-recall context is computed across the full archive. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of June 2026.