Food/Recall·openFDA/food

Ukrop's Homestyle Foods LLC — Class II: Bread Pudding with Vanilla Sauce - KIT NET WT 4 LB (1.81Kg) UPC 7 22515 91732 0 Ukrop's Ho

MediumPublished Sep 9, 2026· AI-analyzed Sep 14, 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

Ukrop's Homestyle Foods LLC has initiated a Class II recall for its Bread Pudding with Vanilla Sauce kit (4 lb) due to the presence of metal fragments. The enforcement action is currently classified as ongoing.

Who it affects

This affects Ukrop's Homestyle Foods LLC, retail distributors of the specified 4 lb Bread Pudding kits, and quality assurance personnel responsible for physical hazard prevention in prepared food manufacturing.

Why it matters

The classification of this recall as Class II suggests the FDA has determined the metal fragments pose a remote probability of adverse health consequences or that the consequences are likely temporary/medically reversible. From a regulatory perspective, this indicates a potential failure in the firm's Hazard Analysis and Risk-Based Preventive Controls (HARPC), specifically regarding physical hazard management on the production line.

Practical takeaway

Quality and operations teams should review foreign material detection protocols, including metal detector sensitivity and maintenance schedules. Organizations handling similar prepared food kits should verify supplier controls for multi-component kits to identify potential points of ingress for physical contaminants.

FDA source material

Class II. Reason: Foreign object: metal fragments. Product: Bread Pudding with Vanilla Sauce - KIT NET WT 4 LB (1.81Kg) UPC 7 22515 91732 0 Ukrop's Homestyle Foods, LLC Richmond, VA 23230. Firm: Ukrop's Homestyle Foods LLC (North Chesterfield VA 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.