Food recall

GELLERT GLOBAL GROUP recall: Ruby, Artichoke Hearts Quartered

GELLERT GLOBAL GROUP, of Elizabeth, NJ, recalled Ruby, Artichoke Hearts Quartered. The FDA's reason: “Foreign material (Glass) was found in the product.” The FDA classified it Class II: it could cause temporary or minor harm. The company began the recall voluntarily on May 15, 2026, and the FDA first listed it in its Enforcement Report of July 22, 2026. The recall is still going on.

How serious

Class II

It could cause temporary or minor harm

Why

Metal, plastic, glass or other objects

Status

Ongoing

The recall

Company
GELLERT GLOBAL GROUP (Elizabeth, NJ)
Reason, in FDA's words
“Foreign material (Glass) was found in the product.”
Where it was sold
The adulterated product was sent to the following states. NY,PA,NJ,CT,
Recall began
, by the company
FDA classified it
First in an FDA Enforcement Report
FDA event number
99055

The product recalled

As the FDA describes them, with the codes that tell whether a package is part of the recall.

  • H-1176-2026 Class II

    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 .

    Codes: P: 25/06/2026 BN: 186/2A E: 24/06/2028 Q.A NG

    Quantity: 1,150 cases

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Source and notes

U.S. Food and Drug Administration, Enforcement Reports (openFDA food recall data) (Public domain (U.S. government work); source U.S. Food and Drug Administration, openFDA), data as of July 22, 2026.

Each week the FDA lists the recalls it has classified in its Enforcement Report, often weeks after the company announced the recall, so a month with five weekly reports tends to count more. Each recall counts once, however many products it covers, in the month FDA first listed it. Class I means the food could cause serious harm or death, Class II temporary or minor harm, and Class III is unlikely to harm anyone. Meat, poultry and most egg products are recalled by the U.S. Department of Agriculture, not the FDA, and aren't included. For what to do with a recalled product, see the FDA's recalls page.