Food/Recall·openFDA/food

SHEANDRO LLC — Class II: Vodka Tomato Sauce, NET WT. 24 oz / 680g, glass jar packed 12 jars in a carton.

MediumPublished Aug 19, 2026· AI-analyzed Aug 25, 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

SHEANDRO LLC has initiated a Class II recall for its Vodka Tomato Sauce (24 oz glass jars) due to the failure to declare milk as an allergen. The product label listed cream and cheese but omitted the mandatory milk allergen declaration.

Who it affects

This recall affects SHEANDRO LLC, food manufacturers utilizing dairy-based ingredients, and regulatory or quality compliance teams responsible for labeling accuracy in the food industry.

Why it matters

The omission of a major allergen declaration constitutes a regulatory failure that necessitates a Class II recall. This suggests a potential gap in the firm's labeling review process or ingredient hazard analysis, specifically regarding the identification of allergens within multi-component ingredients like cream and cheese. For industry professionals, this highlights the necessity of ensuring that common names of ingredients (like 'cheese') are accompanied by the specific required allergen source (in this case, 'milk') if not already clear.

Practical takeaway

Verify all allergen declarations on finished product labels against the raw material specifications for ingredients such as cream and cheese. Quality teams should conduct a label-to-ingredient reconciliation to ensure all sub-components of compound ingredients are correctly identified as allergens.

FDA source material

Class II. Reason: Label declares cream and cheese, but Milk is not declared. Product: Vodka Tomato Sauce, NET WT. 24 oz / 680g, glass jar packed 12 jars in a carton.. Firm: SHEANDRO LLC (Venice FL United States). Status: Ongoing.

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