Recall of Pepsin 1:3000 Powder Due to Potential Salmonella Contamination
Areazine synthesizes this FDA recall directly from FDA's official public data feed. See our methodology for full source attribution and refresh cadence.
American Laboratories, LLC is voluntarily recalling 468 kg of Pepsin 1:3000 Powder because of potential Salmonella contamination, affecting wholesale accounts in several U.S. states and Australia.
What this FDA recall tells you, and what most readers miss
This notice was issued by FDA on April 7, 2026 and geographically references United States. Its severity classification of "medium" signals how the issuing agency weighs the risk of harm if no action is taken - "critical" and "high" tier alerts typically carry direct consumer actions, while "medium" and "low" tend toward informational guidance or monitoring advisories. The category it belongs to - FDA Recalls - determines the consumer-protection framework behind it, which shapes what remedies (refunds, replacements, repairs, or the recall itself) are available to affected consumers and which agency holds statutory responsibility for enforcement.
Most readers skim a notice like this, check whether they are personally affected, and move on. The more useful lens is to verify its scope, source, and timestamp, then compare related notices without assuming that one record proves a broader trend.
Areazine pairs this record with the original agency URL so you can check the primary source before acting. Its related labels are recall, product-safety, cpsc, Food.
What Happened
American Laboratories, LLC is recalling Pepsin 1:3000 Powder due to potential Salmonella contamination. This voluntary recall was initiated on February 26, 2026.
Which Products Are Affected
The affected product is Pepsin 1:3000 Powder, 50 kg, Item #FTI-G0193-00, manufactured by American Laboratories at 5036 South 33rd Street, Omaha, Nebraska 68107. A total of 468 kg is involved, with Manufacturing code: 001, Lot Code: 00160041, and Reevaluation date: February 2, 2029. The product was distributed to 11 direct wholesale accounts in AZ, CA, FL, MO, NM, OH, SC, UT, WI, and 1 direct wholesale account in Australia.
What You Should Do
Consumers who have this product should stop using it immediately and contact American Laboratories, LLC for instructions on returns or refunds. The firm can be reached at their address: 5020 S 33rd St, Omaha, NE 68107-2574.
Why This Matters
This recall addresses a potential health risk from Salmonella, which could lead to foodborne illness, highlighting the importance of product safety in the food supply chain.
Source
This information is from the FDA recall with number H-0612-2026.
Original source: FDA Official Notice ↗
Related FDA Recalls
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Two Areazine-derived peer sets for this FDA recall: nearest notices by body length and by same severity near the same agency date. Peers come from other categories so they are not the same-feed Related list above.
Similar body length
Nearest notices by article body length (1,155 characters here).
Similar severity timing
Same severity (medium) notices issued closest in time to April 7, 2026.
Frequently Asked Questions
Common questions about this FDA recall.