Joy Salty Lassi Recall Issued for 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.
Joy Gourmet Foods LLC is recalling Joy Salty Lassi 16 oz. because the product was not adequately pasteurized. The Class II recall affects 50 gallons distributed in NY, NJ, and PA.
What this FDA recall tells you, and what most readers miss
This notice was issued by FDA on August 4, 2026 and geographically references NY, NJ, PA. 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 Joy Gourmet Foods LLC. initiated a voluntary recall because the product was not adequately pasteurized.
Which Products Are Affected Joy Salty Lassi 16 oz., UPC 68061710010, expiry dates June 30 through July 30, 2026. A total of 50 gallons were distributed in NY, NJ, and PA. Recall number H-1084-2026.
What You Should Do Consumers should not consume the recalled product.
Why This Matters This is an ongoing Class II recall involving a food product that may pose temporary or reversible adverse health consequences.
Source FDA recall H-1084-2026, report date 20260701.
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 (606 characters here).
Similar severity timing
Same severity (medium) notices issued closest in time to August 4, 2026.
Frequently Asked Questions
Common questions about this FDA recall.