FDA recall, , Moderate risk
Ruby Artichoke Hearts Quartered
Artichoke hearts contain foreign material (glass).
Summary by Recall Canary from the FDA notice
What happened
GELLERT GLOBAL GROUP, of Elizabeth, New Jersey, recalled Ruby brand Artichoke Hearts Quartered after foreign material (Glass) was found in the product. The recall began May 15, 2026, and was classified by the FDA on July 14, 2026, covering 1,150 cases. The product was distributed to Connecticut, New Jersey, New York, and Pennsylvania.
The recalled item is a 5 LB 8 OZ (2500 G) can with a drained weight of 3 LBS 6 OZ (1550G), packed six cans per case. The notice states to store in dry conditions. The FDA added the recall to its Enforcement Report on July 14, 2026, and it was in the weekly enforcement report on July 22, 2026.
What to do
We don't have product-specific instructions for this recall. FDA's general advice for food recalls:
- Return it to the store where you bought it, or throw it away.
- Don't give it to anyone else, such as a food bank, or to a pet.
Is your can affected?
Compare these details with yours, then check the recall notice to see which units are recalled.
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 .
Recall details
- Company began the recall
- Sold in
The adulterated product was sent to the following states. New York,Pennsylvania,New Jersey,Connecticut,
- Company
- GELLERT GLOBAL GROUPElizabeth, New Jersey
- Hazard
- Foreign object
- Risk
Moderate risk
Eating it may cause short-term health problems, or ones that treatment can reverse. Serious harm is unlikely.
FDA Class II recall · How risk is rated
- Event ID
- 99055
- Recall number
- H-1176-2026
- Quantity recalled
- 1,150 cases
All recalls from GELLERT GLOBAL GROUP
Timeline
FDA's Enforcement Report is its public list of recalls; FDA adds a recall when it posts it and publishes the list weekly.
Company began the recall
Added to FDA's Enforcement Report · Classified by FDA
Listed on Recall Canary
In FDA's weekly enforcement report
Summary updated
