RECALL RECORD — CLASS IIIRecall closedF-1456-2012/FDA enforcement

Northern Catch Fancy Whole Oysters NET WT

What you need to know

Class III
  • What happened

    Inspectional evidence and sample analyses as well as reports of food borne illness outbreaks due to norovirus have led FDA to believe that Korean molluscan shellfish and…

  • Health risk

    The product is unlikely to cause adverse health consequences. These recalls are often related to labeling or quality violations. An unlabeled prescription or controlled substance was found in a product sold as food or a supplement.

  • Action required

    Check the identifying codes below and stop using the product. Return it to the retailer for a refund or dispose of it safely, following the recall notice.

Recall closed · classified by the FDANationwide (US)More food

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Product identification

Source: FDA FOOD

Brand nameCamerican International
Recalling firmCamerican InternationalParamus, NJ, United States
UPC / barcodesNo UPC listed in the FDA enforcement record.
Lot / date codes
  • OBYL MY7 0427, OBYL MY7 0503, OBYL MY7 0507, OBYL MY7 0512, OBYL MY7 0515, OBYL MY7 0518, OBYL MY7 0519, OBYL MY7 0521, OBYL MY7 0524, OBYL MY39 0505, OBYL MY39 0506, OBYL MY39 0511, OBYL MY39 0513, OBYL SY7 0422, OBYL SY7 0429, OBYL SY7 0521, OBYL SY7 0524, OBYL SY7 0525, OBYL SY39 0510, OBYL SY39 0512, OBYL TY7 0426, OBYL TY7 0427, OBYL TY7 0501, OBYL TY7 0521
Distribution area
Nationwide

Nationwide

United States

Quantity affected95000 units
Recall initiationFDA report date: June 27, 2012
FDA recall numberF-1456-2012

Beyond the headline

The recall, in context

Camerican International initiated this food recall on May 29, 2012. The FDA enforcement report states: Inspectional evidence and sample analyses as well as reports of food borne illness outbreaks due to norovirus have led FDA to believe that Korean molluscan shellfish and products containing KMS as ingredients are adulterated under Section 40(a)(4) in that they were prepared and held under insanitary conditions, whereby they may have become contaminated with filth or whereby they may have been rend. The FDA report lists distribution as: Nationwide.

The FDA enforcement report describes the reason as: Inspectional evidence and sample analyses as well as reports of food borne illness outbreaks due to norovirus have led FDA to believe that Korean molluscan shellfish and products containing KMS as ingredients are adulterated under Section 40(a)(4) in that they were prepared and held under insanitary conditions, whereby they may have become contaminated with filth or whereby they may have been rend

Northern Catch Fancy Whole Oysters NET WT was made or distributed by Camerican International in Paramus, NJ, United States. This page reflects FDA report F-1456-2012, dated June 27, 2012.

Why this is a Class III recall

Class III means the product is unlikely to cause adverse health consequences. These recalls are often related to labeling or quality violations. In this recall, an unlabeled prescription or controlled substance was found in a product sold as food or a supplement.

FDA definition

The product is unlikely to cause adverse health consequences. These recalls are often related to labeling or quality violations.

What to do now

  1. 1

    Stop using it

    Do not eat, drink or take the affected product.

  2. 2

    Check the codes

    Compare the lot and date codes against the table above.

  3. 3

    Return or discard

    Contact the retailer or recalling firm about a refund, and dispose of the product safely.

Consumer safety guide

Product safety recall

Symptoms to watch for

The official enforcement report describes the specific risk. Follow the recall notice, check the product codes and do not use a product that may be affected.

Higher-risk groups

Children, pregnant people, older adults and people with weakened immune systems should take extra care when a product's safety is uncertain.

What to do now

  1. 1Stop using or eating the product and keep it away from children and pets.
  2. 2Check the UPC and lot/date codes on this page and follow the official recall notice for disposal or return.
  3. 3Seek medical advice if anyone develops severe or worrying symptoms after exposure.

Read the official source record for the specific hazard and instructions.

This is general consumer safety information, not medical advice or a diagnosis. Follow the official recall notice and contact a healthcare professional if you have concerns about exposure or symptoms.

Frequently asked

Questions about this recall

What is the Northern Catch Fancy Whole Oysters NET WT recall?

Camerican International recalled Northern Catch Fancy Whole Oysters NET WT in an FDA Class III enforcement action reported as F-1456-2012. Inspectional evidence and sample analyses as well as reports of food borne illness outbreaks due to norovirus have led FDA to believe that Korean molluscan shellfish and…

What should I do if I bought this product?

Check the identifying codes below and stop using the product. Return it to the retailer for a refund or dispose of it safely, following the recall notice. Stop using or eating the product and keep it away from children and pets. Check the UPC and lot/date codes on this page and follow the official recall notice for disposal or return. Seek medical advice if anyone develops severe or worrying symptoms after exposure.

Is the Camerican International recall still active?

The FDA lists this recall as recall closed. It remains relevant if you still have the affected product or need to identify a historical recall.

Where can I verify this recall?

This page is normalized from the openFDA enforcement record F-1456-2012. You can verify it directly using the official source link on this page. VerifyRecall updates its index from public FDA enforcement data and does not replace advice from the FDA, the recalling firm or a healthcare professional.

Verify before you act.

VerifyRecall is independent and not affiliated with the FDA. Always confirm the latest status on the official source record.

Official source

Brand history

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Record last synced from official openFDA enforcement data on November 14, 2026. Source record: official FDA notice.