CLASS I ONGOING Food recall · Reported 17 Dec 2025 · FDA Enforcement Report

Oven Dried Fish (Scomberomorus Cavalla) recalled

African Food on Wheels is recalling Oven Dried Fish (Scomberomorus Cavalla), distributed in New York. The recall was initiated on 5 Nov 2025 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesNo codes
Quantity recalled20 Boxes

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-0237-2026
FDA event ID
97940
Recalling firm
African Food on Wheels, Bronx, NY
Brand
Oven
Classification
Class I
Status
Ongoing
Recall initiated
5 Nov 2025
FDA classified
5 Dec 2025
Reported
17 Dec 2025
Type
Voluntary: Firm initiated
Customers notified by
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Reason category
Botulism
Product category
Fish

Timeline

5 Nov 2025Recall initiated by company
5 Dec 2025Classified by FDA+30 days
17 Dec 2025Published in enforcement report+12 days

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

Reason for recall

Clostridium botulinum (uneviscerated fish)

Product as listed by the FDA

Oven Dried Fish (SCOMBEROMORUS CAVALLA); distributed to walk-in customers of African Food on Wheels Inc. located at 1376 Randall Avenue, Bronx, NY 10474 only; Product is packed in a corrugated brown box.

Where it was distributed

Distributed to walk-in customers of African Food on Wheels Inc. located at 1376 Randall Avenue, Bronx, NY 10474 only

New York

Questions about this recall

Why was it recalled?

Clostridium botulinum (uneviscerated fish)

Which lots are affected?

No codes

Where was it sold?

Distributed to walk-in customers of African Food on Wheels Inc. located at 1376 Randall Avenue, Bronx, NY 10474 only

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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