Fresh Recalls

FDAClass II · Food · Recall H-1176-2026 · Recalled July 22, 2026

Ruby recall — GELLERT GLOBAL GROUP

Agency report date: July 22, 2026.

1. Compare your item

This notice names a product; your particular item is not yet verified. Compare every applicable model, serial, lot, production-date or model-year boundary below.

Product named
Ruby
Company / brand
GELLERT GLOBAL GROUP
Lot / serial / date codes
P: 25/06/2026 BN: 186/2A E: 24/06/2028 Q.A NG
Distribution
The adulterated product was sent to the following states. NY,PA,NJ,CT,
Agency product description and boundaries

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 .

Still to verify: match the label on your item with the full official notice, including any exclusions, tables and photos. Some identifiers appear only on the agency website and are absent from this data feed. A missing field does not mean all versions are affected.

If your lot or date falls outside a stated range, this notice has not established that your item is affected. This is not a finding about other recalls or product safety.

2. Agency hazard and consumer action

FDA reports: Foreign material (Glass) was found in the product.

No consumer remedy instructions are supplied in this record. Check the official notice and listed company contact for the agency’s current instructions.

Class II: may cause temporary or medically reversible health consequences.

Affected product: Ruby

3. Open the official notice or contact

Official recall ID
H-1176-2026
Brand
GELLERT GLOBAL GROUP
Classification
Class II
Units affected
1,150 cases
Recall status
Ongoing
Initiated
Voluntary: Firm initiated

Affected products

Companies & origin

Recalling firm location
Elizabeth, NJ, United States
Firm address
1 Atalanta Plz, 07206

Identifying details (verbatim from the notice)

Product codes / lots
P: 25/06/2026 BN: 186/2A E: 24/06/2028 Q.A NG
Distribution
The adulterated product was sent to the following states. NY,PA,NJ,CT,
Firm notified the public via
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
FDA event ID
99055
Recall initiated
May 15, 2026
FDA classified
July 14, 2026
FDA report date
July 22, 2026
Verify with the official sources:

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Source: U.S. Food & Drug Administration. Agency excerpts come from the public data feed and may omit tables or later changes; the linked government source is authoritative. Source last checked September 7, 2026 at 6:00 AM UTC. Record retrieved September 7, 2026 at 6:00 AM UTC.

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