Food/Recall·openFDA/food

GELLERT GLOBAL GROUP — Class II: Ruby, Artichoke Hearts Quartered, 5 LB 8 OZ (2500 G) DRAINED WT 3 LBS 6 OZ (1550G), Can, 6

MediumPublished Jul 22, 2026· AI-analyzed Jul 27, 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

Gellert Global Group has initiated a Class II recall for Ruby brand Quartered Artichoke Hearts due to the presence of foreign material, specifically glass, found within the product. The recall affects 6-can cases of the 5 lb 8 oz product size and is currently ongoing.

Who it affects

This recall affects Gellert Global Group, commercial food service providers or retailers carrying Ruby brand canned artichokes, and food safety and quality assurance professionals responsible for canned vegetable supply chains.

Why it matters

A Class II designation indicates that the product may cause temporary or medically reversible adverse health consequences, or that the probability of serious adverse health consequences is remote. The presence of glass suggests a potential failure in physical hazard controls during the canning or manufacturing process, which may necessitate an investigation into the firm's supplier verification or production line integrity.

Practical takeaway

QA teams should verify if any inventory from this firm or product line is currently in stock. Manufacturing and packaging leads should review foreign material detection protocols for canned goods to ensure glass contamination risks are mitigated at the production or packing stage.

FDA source material

Class II. Reason: Foreign material (Glass) was found in the product.. Product: Ruby, Artichoke Hearts Quartered, 5 LB 8 OZ (2500 G) DRAINED WT 3 LBS 6 OZ (1550G), Can, 6 cans per case, Store in dry conditions .. Firm: GELLERT GLOBAL GROUP (Elizabeth NJ 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.