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Lower risk Food recall · FDA · Published February 26, 2026

American Laboratories Pepsin 1:3000 Powder Recall: Salmonella Risk

American Laboratories recalls 50kg Pepsin 1:3000 Powder (Item #FTI-G0193-00) due to potential Salmonella contamination. Consumers should check product details and contact the company for guidance.

🇺🇸 FDA recall #H-0612-2026FoodAmerican Laboratories ›
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Contact the company

Recalling firmAmerican Laboratories, LLC5020 S 33rd St · Omaha, NE 68107-2574
✎ GovInfoNow plain-language explainer

American Laboratories is recalling 50kg Pepsin 1:3000 Powder (Item #FTI-G0193-00) because it may contain Salmonella. This poses a food safety risk that could lead to illness if consumed. Read more at govinfonow.com/recall/6691-american-laboratories-pepsin-1-3000-powder-recall-salmonella-risk.

Source Summary by GovInfoNow · govinfonow.com/recall/6691-american-laboratories-pepsin-1-3000-powder-recall-salmonella-risk · Updated August 18, 2026 · Official notice: FDA #H-0612-2026

Cite this page

“American Laboratories Pepsin 1:3000 Powder Recall: Salmonella Risk.” GovInfoNow, updated August 18, 2026. https://govinfonow.com/recall/6691-american-laboratories-pepsin-1-3000-powder-recall-salmonella-risk. Based on FDA recall #H-0612-2026.

The FDA announced on Feb. 26, 2026, that American Laboratories, LLC is recalling Pepsin 1:3000 Powder due to potential Salmonella contamination. The company initiated the voluntary Class II recall.

How to tell if you have it

  • Brand: American Laboratories
  • Product: Pepsin 1:3000 Powder, 50 kg
  • Item #: FTI-G0193-00
  • Manufacturing code: 001
  • Lot Code: 00160041

The hazard

The product poses a potential Salmonella contamination risk. The FDA classified the recall as Class II.

Context

GovInfoNow's records show other recent recalls of similar products include California Dairies Buttermilk Powder Recall (2026-04-20) and California Dairies Low Heat Non-Fat Dried Milk Powder Recall (2026-04-20). PS Save A Lot Bind 50# Seasoning Recall was also reported on 2026-04-22.

How to tell if you have this one

Check for the product name 'Pepsin 1:3000 Powder', 50 kg, and item number #FTI-G0193-00. The manufacturing code is 001 and lot code 00160041.

  • Brand
    American Laboratories
  • Category
    Food
FDA recall event · 3 products

All 3 products in this recall

FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.

  • Classification
    Class II
  • Status
    Terminated
  • Distribution
    11 direct wholesale accounts located in AZ, CA, FL, MO, NM, OH, SC, UT, WI. 1 direct wholesale account located in Australia.
Recall numberProduct, codes & lotsQuantity
H-0610-2026Pepsin 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.; Manufacturing code: 294 Lot Code: 29460025 Reevaluation date: January 20, 2029400 kg
H-0611-2026Pepsin 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.; Manufacturing code: 005 Lot Code: 00560021 Reevaluation date: January 19, 2029370 kg
H-0612-2026Pepsin 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.; Manufacturing code: 001 Lot Code: 00160041 Reevaluation date: February 2, 2029468 kg
Based on the official FDA remedy

What to do — step by step

  1. Check Product Details

    Look for the product name, 50 kg size, and item number #FTI-G0193-00 on the packaging.

Where it went and when

Where it was distributed

Distributed in 9 states, and outside the U.S.

Alaska: not listedAKMaine: not listedMEVermont: not listedVTNew Hampshire: not listedNHWashington: not listedWAIdaho: not listedIDMontana: not listedMTNorth Dakota: not listedNDMinnesota: not listedMNIllinois: not listedILWisconsin: yesWIMichigan: not listedMINew York: not listedNYRhode Island: not listedRIMassachusetts: not listedMAOregon: not listedORNevada: not listedNVWyoming: not listedWYSouth Dakota: not listedSDIowa: not listedIAIndiana: not listedINOhio: yesOHPennsylvania: not listedPANew Jersey: not listedNJConnecticut: not listedCTCalifornia: yesCAUtah: yesUTColorado: not listedCONebraska: not listedNEMissouri: yesMOKentucky: not listedKYWest Virginia: not listedWVVirginia: not listedVAMaryland: not listedMDDelaware: not listedDEArizona: yesAZNew Mexico: yesNMKansas: not listedKSArkansas: not listedARTennessee: not listedTNNorth Carolina: not listedNCSouth Carolina: yesSCDistrict of Columbia: not listedDCOklahoma: not listedOKLouisiana: not listedLAMississippi: not listedMSAlabama: not listedALGeorgia: not listedGAHawaii: not listedHITexas: not listedTXFlorida: yesFL

FDA distribution: “11 direct wholesale accounts located in AZ, CA, FL, MO, NM, OH, SC, UT, WI. 1 direct wholesale account located in Australia.” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: Arizona, California, Florida, Missouri, New Mexico, Ohio, South Carolina, Utah, Wisconsin.

Recall timeline

FDA terminated this recall 2 months after the firm started it.

1. Firm started the recall: Feb 26, 202612. FDA classified it Class II: Mar 20, 202623. Published in FDA’s Enforcement Report: Apr 1, 202634. FDA terminated the recall: May 8, 202642026
  1. Firm started the recall
  2. FDA classified it Class II
  3. Published in FDA’s Enforcement Report
  4. FDA terminated the recall

Dates from the agency record only; steps without a date are left out.

✎ GovInfoNow

Questions people ask

Is this product safe to use?

The recall states potential Salmonella contamination, so it is not safe to use until the manufacturer provides guidance.

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Where this comes from

The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.

  • Official source: FDA Recall #H-0612-2026 (February 26, 2026)
  • Plain-language summary written by qwen3:4b on August 18, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
  • GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA