Food/Recall·FDA Recalls, Market Withdrawals & Safety Alerts

Kettle Cuisine Issues Allergy Alert For Undeclared Shrimp In Whole Foods Market Kitchen Minestrone Soup

MediumPublished May 21, 2026· AI-analyzed May 24, 2026View original FDA source
AI-generated regulatory interpretation. The four sections below are an analyst-style summary produced by an AI model from the original FDA source. Always verify against the source before any regulatory, clinical, or commercial decision.
What happened

Kettle Cuisine is recalling 24oz units of Whole Foods Market Kitchen Minestrone Soup due to the potential presence of undeclared shrimp. The issue poses a risk of serious or life-threatening allergic reactions for individuals with Crustacean Shellfish allergies.

Who it affects

This recall affects Kettle Cuisine, Whole Foods Market, and consumers with shrimp allergies. It is relevant to professionals in food manufacturing, quality assurance, and retail compliance.

Why it matters

The presence of an undeclared major allergen (shrimp) indicates a likely failure in labeling controls or ingredient segregation. Regulatory teams may view this as a significant safety risk, as undeclared allergens are a primary driver of high-priority food recalls. Operational implications include the need for rigorous cross-contamination audits and label accuracy checks during the packaging process.

Practical takeaway

QA teams should immediately verify inventory against the affected 24oz Whole Foods Market Kitchen Minestrone Soup product and implement a hold. Regulatory and labeling departments should review allergen verification protocols for multi-ingredient products to ensure Crustacean Shellfish is accurately declared.

FDA source material

Kettle Cuisine of Lynn, MA is recalling 24oz cups of Whole Foods Market Kitchen Minestrone Soup which may contain undeclared shrimp. People who have allergies to Crustacean Shellfish (Shrimp) run the risk of serious or life-threatening allergic reaction if they consume this product.

Open in openFDA / FDA.gov
AI-generated interpretation. Always verify critical decisions against the original FDA source. Generated with google/gemini-3-flash-preview.