Fresh Recalls

FDAClass I · Food · Recall H-0941-2026 · Recalled June 17, 2026

Individual Unit Label (both lid and front of cup) recall — Kettle Cuisine, LLC

Agency report date: June 17, 2026.

1. Compare your item

This notice names a product; your particular item is not yet verified. Compare every applicable model, serial, lot, production-date or model-year boundary below.

Product named
Individual Unit Label (both lid and front of cup)
Company / brand
Kettle Cuisine
Lot / serial / date codes
Use by: 05/27/26 Lot/Unit Numbers: 1762181 UPC Codes: 099482502065
Distribution
AL, CT, DC, FL, GA, MA, MD, ME, MS, NC, NH, NJ, NY, PA, RI, SC, TN, VA
Agency product description and boundaries

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.

Still to verify: match the label on your item with the full official notice, including any exclusions, tables and photos. Some identifiers appear only on the agency website and are absent from this data feed. A missing field does not mean all versions are affected.

If your lot or date falls outside a stated range, this notice has not established that your item is affected. This is not a finding about other recalls or product safety.

2. Agency hazard and consumer action

FDA reports: Contains undeclared allergen (shrimp).

No consumer remedy instructions are supplied in this record. Check the official notice and listed company contact for the agency’s current instructions.

Class I: most serious — reasonable probability of serious health consequences or death.

Affected product: Individual Unit Label (both lid and front of cup)

3. Open the official notice or contact

Official recall ID
H-0941-2026
Brand
Kettle Cuisine
Classification
Class I
Units affected
562 cases (4,496 - 24oz units)
Recall status
Ongoing
Initiated
Voluntary: Firm initiated

Affected products

Companies & origin

Recalling firm location
Lynn, MA, United States
Firm address
330 Lynnway, N/A, 01901-1706

Identifying details (verbatim from the notice)

Product codes / lots
Use by: 05/27/26 Lot/Unit Numbers: 1762181 UPC Codes: 099482502065
Distribution
AL, CT, DC, FL, GA, MA, MD, ME, MS, NC, NH, NJ, NY, PA, RI, SC, TN, VA
Firm notified the public via
E-Mail
FDA event ID
99038
Recall initiated
May 19, 2026
FDA classified
June 10, 2026
FDA report date
June 17, 2026
Verify with the official sources:

Found something wrong or missing? Report a data error.

Source: U.S. Food & Drug Administration. Agency excerpts come from the public data feed and may omit tables or later changes; the linked government source is authoritative. Source last checked September 7, 2026 at 6:00 AM UTC. Record retrieved September 7, 2026 at 6:00 AM UTC.

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