Lower riskFood recall · FDA · Published May 15, 2026
Gellert Ruby Artichoke Hearts Recall: Foreign Glass Found in Product
Gellert Global Group recalls Ruby Artichoke Hearts Quartered due to foreign glass found in some products. Consumers should check for the specific lot and follow safety steps.
“Gellert Ruby Artichoke Hearts Recall: Foreign Glass Found in Product.” GovInfoNow, updated August 7, 2026. https://govinfonow.com/recall/6218-gellert-ruby-artichoke-hearts-recall-foreign-glass-found-in-product. Based on FDA recall #H-1176-2026.
The FDA announced on May 15, 2026, that Gellert Global Group is recalling Ruby Artichoke Hearts Quartered due to the presence of foreign glass material. The agency issued recall number H-1176-2026 for the Class II voluntary recall.
How to tell if you have it
Brand: Gellert Global Group
Product: Ruby, Artichoke Hearts Quartered
Size: 5 LB 8 OZ (2500 G) DRAINED WT 3 LBS 6 OZ (1550G)
Packaging: Can, 6 cans per case
Lot Code: BN: 186/2A
Production Date: P: 25/06/2026
Expiration Date: E: 24/06/2028
Units Affected: 1,150 cases
Distribution: NY, PA, NJ, CT
The hazard
The FDA stated that foreign material, specifically glass, was found in the product. The recall is classified as Class II.
Context
GovInfoNow's records show Gellert Global Group has one other recall on record since June 25, 2026: a Kimbap recall for undeclared fish allergen risk issued on that date. Other recent recalls of similar products include Ajinomoto Green Gyoza Dumplings Recall (March 3, 2026), Trader Joe's Vegetable Fried Rice Recall (March 3, 2026), and JFE Dumpling Party Trays Recall (March 5, 2026).
How to tell if you have this one
Check for the product name 'Ruby, Artichoke Hearts Quartered', 5 LB 8 OZ (2500 G) DRAINED WT 3 LBS 6 OZ (1550G), 6 cans per case. The batch number starts with 'P: 25/06/2026 BN: 186/2A'.
Brand
Gellert Global Group
Category
Food
Based on the official FDA remedy
What to do — step by step
Check Product Details
Look for the product name, size, and batch number on the can to confirm if it's affected.
Where it went and when
Where it was distributed
Distributed in 4 states.
Listed by the agency
Not listed
FDA distribution: “The adulterated product was sent to the following states. NY,PA,NJ,CT,” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Connecticut, New Jersey, New York, Pennsylvania.
Recall timeline
FDA published this recall 2 months after the firm started it.
1Firm started the recall
2FDA classified it Class II
3Published in FDA’s Enforcement Report
Dates from the agency record only; steps without a date are left out.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
Official source: FDA Recall #H-1176-2026 (May 15, 2026)
Plain-language summary written by qwen3:4b on August 7, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.