Class IIOngoingVoluntary: Firm initiated
GELLERT GLOBAL GROUP: food recall H-1176-2026
GELLERT GLOBAL GROUP of Elizabeth, NJ 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… Reason: Foreign material (Glass) was found in the product. The FDA listed it as Class II in its Enforcement Report dated Jul 22, 2026; distribution: Connecticut, New Jersey, New York, Pennsylvania.
Record status as published: Ongoing. openFDA data last updated Oct 21, 2026.
Have this product? Check FDA.gov and your retailer. This page reproduces an FDA Enforcement Report record and is not a public alert. Look for the firm's recall notice on the FDA's recalls page, or ask the store where you bought it what to do. If you think you got sick from a food, contact a health care provider.
Recall details
- 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 .
- Product quantity
- 1,150 cases
- Reason for recall
- Foreign material (Glass) was found in the product.
- Codes, lots and dates on the package
- P: 25/06/2026 BN: 186/2A E: 24/06/2028 Q.A NG
- Distribution pattern
- The adulterated product was sent to the following states. NY,PA,NJ,CT,
- Recalling firm
- GELLERT GLOBAL GROUP, Elizabeth, NJ
- Classification
- Class II — the FDA uses this class for a situation in which using or being exposed to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
- Voluntary or mandated
- Voluntary: Firm initiated
- How the firm first notified customers
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Advertisement
Dates
| Event | Date |
|---|---|
| Recall initiated by the firm | May 15, 2026 |
| Classified by the FDA | Jul 14, 2026 |
| Published in the Enforcement Report | Jul 22, 2026 |
Other recalls by GELLERT GLOBAL GROUP
- H-1186-2026 · Jul 29, 2026 · Class I — Undeclared Allergen (Fish)
Advertisement
OpenPlate shows FDA records as published and does not add new findings. Product names and company names belong to their owners.
Sources
- U.S. Food and Drug Administration, openFDA food enforcement reports, recall number H-1176-2026 (openFDA record). Data provided by the U.S. Food and Drug Administration (https://open.fda.gov).
- Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service. The FDA does not endorse OpenPlate.