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Food FDA Class I Ongoing Undeclared allergen

Individual Unit Label (both lid and front of cup): Whole Foods Market Kitchens Minestrone Soup, VEGETARIAN NET WT 24 OZ (1 Lb 8OZ) 680g. Case Label: Whole Foods Global Minestrone Soup 702505, KEEP REFRIGERATED, Distributed by Whole Foods Market Austin, TX 78703. Eight (8)/ 24 oz. Cups (Net Wt. 12 L

Kettle Cuisine, LLC Published Jun 17, 2026

Risk level

Class I

Dangerous or defective — could cause serious health problems or death.

Severity score 92/100

What should you do?

  • Check whether you have this product, using the lot codes, UPCs, and dates listed below.
  • If you are allergic or sensitive to the ingredient noted, do not eat it — it could cause a serious reaction.
  • Return it to the place of purchase for a refund, or throw it away in a sealed bag so people and animals can’t get to it.
  • Contact Kettle Cuisine, LLC or your place of purchase with questions, and see the source record below for full details.
Reason for recall

Contains undeclared allergen (shrimp).

Hazards

Crustacean Shellfish · primary

Affected products (1)

Individual Unit Label (both lid and front of cup): Whole Foods Market Kitchens Minestrone Soup, VEGETARIAN NET WT 24 OZ (1 Lb 8OZ) 680g. Case Label: Whole Foods Global Minestrone Soup 702505, KEEP REFRIGERATED, Distributed by Whole Foods Market Austin, TX 78703. Eight (8)/ 24 oz. Cups (Net Wt. 12 LBS)/case.

562 cases (4,496 - 24oz units)

Code info: Use by: 05/27/26 Lot/Unit Numbers: 1762181 UPC Codes: 099482502065

Affected areas

AlabamaConnecticutDistrict of ColumbiaFloridaGeorgiaMaineMarylandMassachusettsMississippiNew HampshireNew JerseyNew YorkNorth CarolinaPennsylvaniaRhode IslandSouth CarolinaTennesseeVirginia

Timeline

  1. Initiated
    May 19, 2026
  2. Published
    Jun 17, 2026
Recall number
H-0941-2026
Agency
U.S. Food and Drug Administration
Country
US

FDA records come from the openFDA food enforcement-report dataset — the agency's full weekly enforcement list. Most entries are not issued as consumer press releases, so they won't appear on fda.gov/recalls or in a web search. The source record link above resolves this exact recall by its number.