Recall of Pepsin 1:10,000 Powder Due to Potential Salmonella Contamination
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American Laboratories, LLC is voluntarily recalling 370 kg of Pepsin 1:10,000 Powder over 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 and Australia. 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, fda, Food.
Recall of Pepsin 1:10,000 Powder
What Happened
American Laboratories, LLC is recalling its Pepsin 1:10,000 Powder due to potential Salmonella contamination, as part of a voluntary firm-initiated action.
Which Products Are Affected
The affected product is Pepsin 1:10,000 Powder, 10 kg, Item #FTI-G0193-00, packed in double poly-lined cardboard drums or boxes. A total of 370 kg is involved, with manufacturing code 005, Lot Code 00560021, and reevaluation date January 19, 2029. It was distributed to 11 direct wholesale accounts in Arizona, California, Florida, Missouri, New Mexico, Ohio, South Carolina, Utah, and Wisconsin, as well as one direct wholesale account in Australia. The recall number is H-0611-2026.
What You Should Do
Consumers should contact American Laboratories, LLC at 5020 S 33rd St, Omaha, NE 68107-2574 for instructions on returns or refunds, as the recall was initiated via e-mail.
Why This Matters
This recall addresses potential food safety risks from contamination, which could impact public health by causing illness, though the FDA has classified it as Class II, indicating a remote probability of serious consequences.
Source
FDA Recall Number: H-0611-2026. Attribution: FDA (U.S. Food and Drug Administration).
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 (1,264 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.