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High RiskFDAfda-F-1653-2012CONTAMINATION

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

Category
Units Affected
41,810
Recall Date
May 18, 2012
Issuing Agency
Hazard
Contamination

FDA Recall Notice

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for 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 whereby they may have become contaminated with filth, or whereby they have been rendered injurious to health.

Corrective Action (per FDA)

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1653-2012.

Recall terminated by FDA.

✅ What you should do

  1. Stop using the product if you own it.
  2. Check the model number, lot code, or sell-by date against the recall notice above.
  3. Contact Nishimoto Trading Co Ltd or the retailer where you bought it for a refund, replacement, or repair.
  4. For the most current official instructions, visit the FDA recall page.
  5. If you've been hurt by this product, report the incident to FDA.

Consumer Contact (per FDA)

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1653-2012.

Nishimoto Trading Co Ltd

FDA

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The FDA regulates drugs, medical devices, food, cosmetics, and tobacco. Adverse event reports and recall notices are the main public safety signal.

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📣 Report a food, supplement, or cosmetic problem to the FDA

If you had a reaction, found contamination, or experienced a labeling problem with this product, report it to the FDA. The agency uses consumer reports to track emerging safety signals and trigger recalls.

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Nishimoto Trading Co Ltd Recall FAQ

Nishimoto Trading Co Ltd is the subject of a seafood safety report: Oysters Breaded/Kaki Fry, 12x2lbs, item #88250, SK Breaded Oyster 10x2lb, item#91750, and Oyster Breaded Big KOR SK F, item#91306.. The notice was published on May 18, 2012 by the U.S. Food and Drug Administration (FDA). Approximately 41,810 units are potentially affected.