Whole Foods Market Minestrone Soup Recall for Undeclared Shrimp
Areazine synthesizes this FDA recall directly from FDA's official public data feed. See our methodology for full source attribution and refresh cadence.
Kettle Cuisine, LLC is recalling 4,496 units of Whole Foods Market Kitchens Minestrone Soup due to undeclared shrimp allergen.
What this FDA recall tells you, and what most readers miss
This notice was issued by FDA on July 27, 2026 and geographically references United States. Its severity classification of "high" 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
The recall was initiated because the product contains undeclared shrimp.
Which Products Are Affected
Whole Foods Market Kitchens Minestrone Soup, VEGETARIAN, NET WT 24 OZ (1 Lb 8 OZ) 680g. UPC: 099482502065. Use by: 05/27/26. Lot/Unit Numbers: 1762181. Case Label: Whole Foods Global Minestrone Soup 702505. 562 cases (4,496 units) distributed in AL, CT, DC, FL, GA, MA, MD, ME, MS, NC, NH, NJ, NY, PA, RI, SC, TN, VA. Recall number H-0941-2026.
What You Should Do
Consumers who have the product should not consume it if they have a shrimp allergy.
Why This Matters
This is a Class I recall for an undeclared allergen that can cause serious or life-threatening allergic reactions.
Source
FDA recall H-0941-2026, reported June 17, 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 (768 characters here).
Similar severity timing
Same severity (high) notices issued closest in time to July 27, 2026.
Frequently Asked Questions
Common questions about this FDA recall.