Kettle Cuisine, LLC food recall: Individual Unit Label
Key facts
- Agency
- U.S. Food and Drug Administration (FDA)
- Program
- Food
- Classification
- Class I
- Status
- Ongoing
- Event ID
- 99038
- Recall initiated
- May 19, 2026
- Classified by FDA
- Jun 10, 2026
- Posted in Enforcement Report
- Jun 17, 2026
- Recalling firm
- Kettle Cuisine, LLC
- Firm location
- Lynn, MA, United States
- Initiated by
- Voluntary: Firm initiated
- Firm notified customers by
- Products in this event
- 1
What to do
Compare the product name, size, UPC, lot codes and dates below with the product you have. If it matches, do not eat it. Follow the firm's instructions to return it or throw it away.
Reason for recall
Contains undeclared allergen (shrimp).
What the classification means
- Class I: FDA's most serious category: there is a reasonable probability that using or being exposed to the product will cause serious health problems or death.
About this recall
The firm started this recall on May 19, 2026. FDA classified it 22 days later, on Jun 10, 2026. Distribution reported by FDA: AL, CT, DC, FL, GA, MA, MD, ME, MS, NC, NH, NJ, NY, PA, RI, SC, TN, VA Kettle Cuisine, LLC has 3 recalls in our records.
Recalled products (1)
H-0941-2026 Class I Ongoing
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.
Codes / lots: Use by: 05/27/26 Lot/Unit Numbers: 1762181 UPC Codes: 099482502065
Quantity: 562 cases (4,496 - 24oz units)
Source and freshness
- Source
- U.S. Food and Drug Administration (FDA) Enforcement Report, via the openFDA food enforcement dataset
- Official notice
- FDA Enforcement Report, event 99038
- Raw record
- openFDA API (JSON)
- Dataset last updated by FDA
- Nov 3, 2026
- Imported by RecallRadar
- Nov 4, 2026
Enforcement Report entries describe recalls FDA has classified. They are not always the same as a company press release. If something here differs from FDA's record, FDA's record is correct — please tell us.