Mehadrin Chocolate Leben Recall Due to Pasteurization Issue
Areazine synthesizes this FDA recall directly from FDA's official public data feed. See our methodology for full source attribution and refresh cadence.
UPSTATE NIAGARA COOPERATIVE is recalling 3,975 cases of Mehadrin Chocolate Leben after the product may have been improperly pasteurized.
Reading this FDA recall beyond the headline
This notice was issued by FDA on September 8, 2026 and geographically references New Jersey. The FDA classifies this as a Class II recall, with the stated reason "Product may have been improperly pasteurized.", distributed nj. FDA recall classes run from I (reasonable probability of serious harm) to III (unlikely to cause harm), so the class number is the fastest way to gauge severity here. 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.
The original agency source is linked below so you can verify this record directly before acting on it. Its related labels are recall, product-safety, fda, Food.
What Happened
The recalling firm initiated a voluntary recall because the product may have been improperly pasteurized.
Which Products Are Affected
Mehadrin Chocolate Leben, 6 OZ (170g) CUPS, UPC: 070784023144. Lot code: 101426 L5 2W, Use by date: 10/14/26. A total of 3,975 cases are affected. Distribution was limited to NJ.
What You Should Do
Consumers should not consume the affected product. Contact the recalling firm for further instructions regarding return or refund.
Why This Matters
This is a Class II recall involving a potential food safety issue with distribution in New Jersey.
Source
FDA recall number H-1332-2026. Recalling firm: UPSTATE NIAGARA COOPERATIVE, Lancaster, NY.
Original source: FDA Official Notice ↗
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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 (709 characters here).
Similar severity timing
Same severity (medium) notices issued closest in time to September 8, 2026.
Questions & Answers
Questions readers often have about this FDA recall.