CLASS I Food recall · Reported 13 Mar 2019 · FDA Enforcement Report

Wild Dungeness Crab Cake recalled by Southwind Foods

Southwind Foods is recalling Wild Dungeness Crab Cake, distributed in Arizona, California, Hawaii. The recall was initiated on 21 Dec 2018 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesLot #18A337-01; Best by 3-2-2019
Quantity recalled13 cases (156 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-1141-2019
FDA event ID
82047
Recalling firm
Southwind Foods, Long Beach, CA
Classification
Class I
Status
Terminated
Recall initiated
21 Dec 2018
FDA classified
1 Mar 2019
Reported
13 Mar 2019
Type
Voluntary: Firm initiated
Customers notified by
E-Mail
Reason category
Temperature Abuse
Product category
Cakes & Pastries

Timeline

21 Dec 2018Recall initiated by company
1 Mar 2019Classified by FDA+70 days
13 Mar 2019Published 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

Crab meat recalled by supplier due to potential temperature abuse.

Foods that need refrigeration and were stored or shipped too warm can grow harmful bacteria without any change in look or smell.

Product as listed by the FDA

Wild Dungeness Crab Cake; Net Weight: 12 lb - 48 x 4.0 oz. Keep Frozen Manufactured for Whole Foods Market

Where it was distributed

Whole Foods in CA, AZ, HI

ArizonaCaliforniaHawaii

Stores named: Whole Foods

Questions about this recall

Why was it recalled?

Crab meat recalled by supplier due to potential temperature abuse.

Which lots are affected?

Lot #18A337-01; Best by 3-2-2019

Where was it sold?

Whole Foods in CA, AZ, HI

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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