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 c
Summary
The FDA issued a Class II for Ruby, Artichoke Hearts Quartered, 5 LB 8 OZ (2500 G) DRAINED WT 3 LBS 6 OZ (1550 by GELLERT GLOBAL GROUP. Reason: Foreign material (Glass) was found in the product..
Details
Source
Food Recall
External ID
H-1176-2026
Action Date
2026-07-22
Status
Ongoing
Category
food
Product Description
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 .
Lot/Code Info: P: 25/06/2026 BN: 186/2A E: 24/06/2028 Q.A NG
Quantity Affected: 1,150 cases
Reason for Recall
Foreign material (Glass) was found in the product.
Distribution
The adulterated product was sent to the following states. NY,PA,NJ,CT,
Type: Voluntary: Firm initiated
Recall Initiated: 2026-05-15
Company
Elizabeth, NJ
Context & Analysis
This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.
This was one of 39 food recalls issued in the same week, part of 94 food-related FDA actions this month.
Frequently Asked Questions
What is a Class II recall?
A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (GELLERT GLOBAL GROUP) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does GELLERT GLOBAL GROUP have FDA actions?
This is the only FDA action we have on record for GELLERT GLOBAL GROUP in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "H-1176-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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