CLASS II Food recall · Reported 11 Jan 2017 · FDA Enforcement Report

Fresh Catch Smoked Baby Clams recalled by Mitsui Foods

Mitsui Foods is recalling Fresh Catch Smoked Baby Clams. The recall was initiated on 4 Nov 2016 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesLot 508660-001 (Mitsui Foods Lot) WFSBC-160401
Quantity recalled6750 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-0856-2017
FDA event ID
75874
Recalling firm
Mitsui Foods, Norwood, NJ
Classification
Class II
Status
Terminated
Recall initiated
4 Nov 2016
FDA classified
5 Jan 2017
Reported
11 Jan 2017
Type
Voluntary: Firm initiated
Customers notified by
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Reason category
Packaging Defects
Product category
Oysters & Shellfish

Timeline

4 Nov 2016Recall initiated by company
5 Jan 2017Classified by FDA+62 days
11 Jan 2017Published in enforcement report+6 days

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

Reason for recall

A seal quality issue with the packaging may result in the food spoiling causing package swelling (bloating)

Packaging recalls include wrong labels, wrong products in the wrong bottle, missing leaflets, short-filled or empty capsules and seals that fail.

Product as listed by the FDA

Fresh Catch Smoked Baby Clams 3.53 oz. pouch (100g) Item Number 541187381, UPC 087381043895

Where it was distributed

U.S

Questions about this recall

Why was it recalled?

A seal quality issue with the packaging may result in the food spoiling causing package swelling (bloating)

Which lots are affected?

Lot 508660-001 (Mitsui Foods Lot) WFSBC-160401

Where was it sold?

U.S

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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