CLASS II Food recall · Reported 27 Jun 2012 · FDA Enforcement Report

Ocean Green)oyster Large*6, Iqf recalled by Woosung America

Woosung America is recalling Ocean Green)oyster Large*6, Iqf, distributed in California. The recall was initiated on 8 Jun 2012 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesItem number oys0070
Quantity recallednot provided

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-1448-2012
FDA event ID
62273
Recalling firm
Woosung America, Hayward, CA
Brand
Ocean
Classification
Class II
Status
Terminated
Recall initiated
8 Jun 2012
FDA classified
15 Jun 2012
Reported
27 Jun 2012
Type
Voluntary: Firm initiated
Customers notified by
Visit
Reason category
Other Reasons
Product category
Oysters & Shellfish

Timeline

8 Jun 2012Recall initiated by company
15 Jun 2012Classified by FDA+7 days
27 Jun 2012Published 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

The product has been prepared, packed, or held under insanitary conditions whereby it may have become contaminated with filth, or whereby it may have been rendered injurious to health.

Product as listed by the FDA

OCEAN GREEN)OYSTER LARGE 5lb*6, IQF Imported by: J & S Group 2535E 12th St. #B Los Angeles, CA 90021

Where it was distributed

Northern CA only.

California

Questions about this recall

Why was it recalled?

The product has been prepared, packed, or held under insanitary conditions whereby it may have become contaminated with filth, or whereby it may have been rendered injurious to health.

Which lots are affected?

Item number oys0070

Where was it sold?

Northern CA 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 II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

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

3 other products · FDA event 62273

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