Joy Saffron Cardamon Lassi Recall Issued by Joy Gourmet Foods LLC
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Joy Gourmet Foods LLC is recalling Joy Saffron Cardamon Lassi 16 oz. due to inadequate pasteurization.
What this FDA recall tells you, and what most readers miss
This notice was issued by FDA on August 4, 2026 and geographically references New York, New Jersey, Pennsylvania. 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. is recalling the product because it was not adequately pasteurized.
Which Products Are Affected
The recall involves Joy Saffron Cardamon Lassi 16 oz. (UPC 68061710034), with expiry dates June 30 through July 30, 2026. A total of 50 gallons were distributed in NY, NJ, and PA under recall number H-1094-2026.
What You Should Do
Consumers in the affected states should check product expiry dates and avoid consuming the recalled item.
Why This Matters
This Class II recall addresses a potential health risk from inadequate pasteurization in a limited distribution area.
Source
FDA recall H-1094-2026 (https://www.fda.gov)
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 (675 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.