CLASS II ONGOING Food recall · Reported 22 Jul 2026 · FDA Enforcement Report
Ruby, Artichoke Hearts Quartered Drained WT, Store in dry conditions recalled
Gellert Global Group is recalling Ruby, Artichoke Hearts Quartered Drained WT, Store in dry conditions, distributed in Connecticut, New Jersey, New York, Pennsylvania. The recall was initiated on 15 May 2026 and the FDA has classified it as Class II.
Check your package
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
Recall details
- Recall number
- H-1176-2026
- FDA event ID
- 99055
- Recalling firm
- Gellert Global Group, Elizabeth, NJ
- Brand
- Ruby
- Classification
- Class II
- Status
- Ongoing
- Recall initiated
- 15 May 2026
- FDA classified
- 14 Jul 2026
- Reported
- 22 Jul 2026
- Type
- Voluntary: Firm initiated
- Customers notified by
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Reason category
- Foreign Material
- Product category
- Other
Timeline
| 15 May 2026 | Recall initiated by company | |
| 14 Jul 2026 | Classified by FDA | +60 days |
| 22 Jul 2026 | Published in enforcement report | +8 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Foreign material (Glass) was found in the product.
Foreign material recalls cover pieces of metal, plastic, glass, wood or other objects that got into the product during processing and could cause injury if eaten.
Product as listed by the FDA
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 .
Where it was distributed
The adulterated product was sent to the following states. NY,PA,NJ,CT,
Questions about this recall
Is Ruby, Artichoke Hearts Quartered Drained WT, Store in dry conditions recalled?
Yes. Gellert Global Group recalled Ruby, Artichoke Hearts Quartered Drained WT, Store in dry conditions on 15 May 2026. The recall is Class II and its status is Ongoing. Recall number H-1176-2026.
Why was it recalled?
Foreign material (Glass) was found in the product.
Which lots are affected?
P: 25/06/2026 BN: 186/2A E: 24/06/2028 Q.A NG
Where was it sold?
The adulterated product was sent to the following states. NY,PA,NJ,CT,
What should I do if I have it?
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
What does Class II mean?
Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.
Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
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|---|---|---|---|---|---|
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