Pacific American Fish Company (PAFCO) is recalling recalling Korean Oysters because the product has been prepared, packed, or held under insanitary conditions whereby it may…
Health risk
The product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote. A safety issue that does not fit the standard pathogen, allergen, chemical or quality categories.
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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Pacific American Fish Co INC initiated this food recall on June 28, 2012. The FDA enforcement report states: Pacific American Fish Company (PAFCO) is recalling recalling Korean Oysters because 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. The FDA report lists distribution as: Nationwide in the US.
The FDA enforcement report describes the reason as: Pacific American Fish Company (PAFCO) is recalling recalling Korean Oysters because 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.
Brd Oyster (Kaki) Iqf Farm, Brd 106, 12/2lbs was made or distributed by Pacific American Fish Co INC in Vernon, CA, United States. This page reflects FDA report F-1794-2012, dated August 1, 2012.
Why this is a Class II recall
Class II means the product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote. In this recall, a safety issue that does not fit the standard pathogen, allergen, chemical or quality categories.
FDA definition
The product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote.
What to do now
1
Stop using it
Do not eat, drink or take the affected product.
2
Check the codes
Compare the lot and date codes against the table above.
3
Return or discard
Contact the retailer or recalling firm about a refund, and dispose of the product safely.
Consumer safety guide
Undeclared fish
Symptoms to watch for
Hives, swelling, wheezing, vomiting or anaphylaxis can occur in people with a fish allergy.
When symptoms may appear
Reactions can begin within minutes to a few hours after eating the product.
Higher-risk groups
People with a diagnosed fish allergy, especially anyone with a history of anaphylaxis.
What to do now
1Do not eat the product if you have a fish allergy.
2Seek emergency care for breathing difficulty, throat swelling or other signs of anaphylaxis.
3Keep the packaging and contact the retailer or manufacturer about a refund.
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
4 answers
What is the Brd Oyster (Kaki) Iqf Farm, Brd 106, 12/2lbs recall?
Pacific American Fish Co INC recalled Brd Oyster (Kaki) Iqf Farm, Brd 106, 12/2lbs in an FDA Class II enforcement action reported as F-1794-2012. Pacific American Fish Company (PAFCO) is recalling recalling Korean Oysters because the product has been prepared, packed, or held under insanitary conditions whereby it may…
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. Do not eat the product if you have a fish allergy. Seek emergency care for breathing difficulty, throat swelling or other signs of anaphylaxis. Keep the packaging and contact the retailer or manufacturer about a refund.
Is the Pacific American Fish Co INC 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-1794-2012. 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.