CLASS I Food recall · Reported 9 Nov 2022 · FDA Enforcement Report

Halibut (fillets and portions) recalled by Mariscos Bahia

Mariscos Bahia is recalling Halibut (fillets and portions), distributed in Arizona, California. The recall was initiated on 20 Oct 2022 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesProduct code: HALL, HALP, HALP8
Quantity recalled5,718.23 lbs.

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
F-0084-2023
FDA event ID
91036
Recalling firm
Mariscos Bahia, Pico Rivera, CA
Brand
Halibut
Classification
Class I
Status
Terminated
Recall initiated
20 Oct 2022
FDA classified
2 Nov 2022
Reported
9 Nov 2022
Type
Voluntary: Firm initiated
Customers notified by
E-Mail
Reason category
Salmonella
Product category
Fish

Timeline

20 Oct 2022Recall initiated by company
2 Nov 2022Classified by FDA+13 days
9 Nov 2022Published 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

Possible contamination with salmonella

Salmonella causes fever, diarrhea and abdominal cramps, usually 12 to 72 hours after eating contaminated food. Most people recover without treatment, but severe cases can need hospital care.

Product as listed by the FDA

Halibut (fillets and portions) packed in 10-50 lb. corrugated cardboard or Styrofoam boxes

Where it was distributed

Product was distributed to 179 customers located in Arizona and California. The firm utilizes 3 distributors in California and 2 in Arizona. End users are primarily restaurants.

ArizonaCalifornia

Questions about this recall

Why was it recalled?

Possible contamination with salmonella

Which lots are affected?

Product code: HALL, HALP, HALP8

Where was it sold?

Product was distributed to 179 customers located in Arizona and California. The firm utilizes 3 distributors in California and 2 in Arizona. End users are primarily restaurants.

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.

Other products in this recall event

6 other products · FDA event 91036

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