Recall of Pepsin Full Strength 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 400 kg of Pepsin Full Strength 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 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.
What Happened
American Laboratories, LLC is recalling Pepsin Full Strength Powder due to potential Salmonella contamination, as announced in a voluntary firm-initiated recall.
Which Products Are Affected
The affected product is Pepsin Full Strength Powder, 50 kg, Item #5000545, manufactured by American Laboratories at 5036 South 33rd Street, Omaha, Nebraska 68107. The recall involves a total of 400 kg, with the specific code information including Manufacturing code: 294, Lot Code: 29460025, and Reevaluation date: January 20, 2029. It is packed in double poly-lined cardboard drums or boxes. Distribution occurred to 11 direct wholesale accounts in the states of AZ, CA, FL, MO, NM, OH, SC, UT, and WI in the United States, as well as 1 direct wholesale account in Australia. The official recall number is H-0610-2026.
What You Should Do
Consumers who have this product should stop using it immediately and contact American Laboratories, LLC at their address, 5020 S 33rd St, Omaha, NE 68107-2574, for instructions on returns or refunds, as the initial firm notification was made via e-mail.
Why This Matters
This recall addresses potential health risks from Salmonella contamination, which could lead to temporary adverse effects, highlighting the importance of food safety in manufacturing and distribution.
Source
Source: FDA, recall number H-0610-2026.
Original source: FDA Official Notice ↗
Related FDA Recalls
All FDA Recalls →Nationwide notices with similar length or severity timing 8
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 (1,380 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.