CLASS I ONGOING Food recall · Reported 26 Nov 2025 · FDA Enforcement Report

Dry Ghoinnya Fish recalled by New Hoque and Sons

New Hoque and Sons is recalling Dry Ghoinnya Fish, distributed in New Jersey, New York. The recall was initiated on 28 Oct 2025 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesExpiration date of 5/19/25 UPC code is 908172635412.
Quantity recalled5 cases (10 - 12 lbs. per case)

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-0202-2026
FDA event ID
97895
Recalling firm
New Hoque and Sons, Maspeth, NY
Classification
Class I
Status
Ongoing
Recall initiated
28 Oct 2025
FDA classified
19 Nov 2025
Reported
26 Nov 2025
Type
Voluntary: Firm initiated
Customers notified by
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Reason category
Other Reasons
Product category
Fish

Timeline

28 Oct 2025Recall initiated by company
19 Nov 2025Classified by FDA+22 days
26 Nov 2025Published in enforcement report+7 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Un-eviscerated fish may be contaminated with Clostridia botulinum.

Product as listed by the FDA

Dry Ghoinnya Fish

Where it was distributed

NY, NJ

New JerseyNew York

Questions about this recall

Why was it recalled?

Un-eviscerated fish may be contaminated with Clostridia botulinum.

Which lots are affected?

Expiration date of 5/19/25 UPC code is 908172635412.

Where was it sold?

NY, NJ

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 I mean?

Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.

Read the official FDA notice · Source record retrieved 26 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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