CLASS III Food recall · Reported 14 Apr 2021 · FDA Enforcement Report

Crimson Snapper Fillet, Natural Cut CO Treated recalled by Sea World

Sea World is recalling Crimson Snapper Fillet, Natural Cut CO Treated, distributed in Puerto Rico. The recall was initiated on 22 Mar 2021 and the FDA has classified it as Class III.

Check your package

Lot, batch or date codesLot # 04008850981, Best by Date: 11-27-2022, Item # 307353
Quantity recalled298 cases

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-0436-2021
FDA event ID
87571
Recalling firm
Sea World, San Juan, PR
Classification
Class III
Status
Terminated
Recall initiated
22 Mar 2021
FDA classified
20 Apr 2021
Reported
14 Apr 2021
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
Other

Timeline

22 Mar 2021Recall initiated by company
14 Apr 2021Published in enforcement report+23 days
20 Apr 2021Classified by FDA+6 days

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

Reason for recall

Fish decomposition.

Product as listed by the FDA

Crimson Snapper Fillet, Natural Cut CO Treated, Net WT 10 LBS, Size 10/12 oz

Where it was distributed

Domestic distribution only-PR

Puerto Rico

Questions about this recall

Why was it recalled?

Fish decomposition.

Which lots are affected?

Lot # 04008850981, Best by Date: 11-27-2022, Item # 307353

Where was it sold?

Domestic distribution only-PR

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 III mean?

Class III recalls are for products unlikely to cause any adverse health consequence, usually labelling or quality issues.

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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