FDA recall record

Nishimoto Trading Co Oysters Breaded/Kaki Fry, 12x2lbs, item #88250, SK Breaded recall — FDA F-1653-2012

Nishimoto is recalling all Shirakiku Brand Oyster Breaded received from Korea because they have been prepared, packed, or held under insanitary conditions…

Class IIclassification
F-1653-2012official record ID
Jul 4, 2012report date

Recall record at a glance

Official recordF-1653-2012
CategoryFood Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmNishimoto Trading Co Ltd
Report dateJul 4, 2012
Recall initiation dateMay 18, 2012
Quantity41,810 units
LocationSanta Fe Springs, CA, United States

Official product description

Oysters Breaded/Kaki Fry, 12x2lbs, item #88250, SK Breaded Oyster 10x2lb, item#91750, and Oyster Breaded Big KOR SK F, item#91306.

Why the product was recalled

Nishimoto is recalling all Shirakiku Brand Oyster Breaded received from Korea because they have been prepared, packed, or held under insanitary conditions whereby they may have become contaminated with filth, or whereby they have been rendered injurious to health.

Distribution information

Nationwide in the US

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

FDA source limitation: openFDA enforcement reports are a reference dataset, not a live public-alert or recall-lifecycle service. FDA notes that enforcement-report status may not be updated after classification. Confirm current actions with the FDA, recalling firm or appropriate healthcare professional when relevant.