CLASS II Food recall · Reported 18 Jul 2012 · FDA Enforcement Report

Clams, Frozen Boiled Baby, in shell packages, 24 pkgs/carton recalled

Rhee Brothers is recalling Clams, Frozen Boiled Baby, in shell packages, 24 pkgs/carton, distributed nationwide in the US. The recall was initiated on 1 Jun 2012 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesProduct is not date coded.
Quantity recalled211

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-1728-2012
FDA event ID
62492
Recalling firm
Rhee Brothers, Hanover, MD
Brand
Clams
Classification
Class II
Status
Terminated
Recall initiated
1 Jun 2012
FDA classified
6 Jul 2012
Reported
18 Jul 2012
Type
Voluntary: Firm initiated
Customers notified by
Letter
Reason category
Norovirus
Product category
Oysters & Shellfish

Timeline

1 Jun 2012Recall initiated by company
6 Jul 2012Classified by FDA+35 days
18 Jul 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

Frozen clams, product of S. Korea, may be contaminated with Norovirus.

Product as listed by the FDA

Clams, Frozen Boiled Baby, in shell, 10 oz packages, 24 pkgs/carton, item #20699K. UPC 081652 206996.

Where it was distributed

The product was distributed nationwide.

Nationwide

Questions about this recall

Why was it recalled?

Frozen clams, product of S. Korea, may be contaminated with Norovirus.

Which lots are affected?

Product is not date coded.

Where was it sold?

The product was distributed nationwide.

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.

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