🔍 RecallPedia

Frozen Oysters: 1) CHORIPDONG) FROZEN OYSTER, IQF 8OZ*40; 2) CJ FOOD, INC.)FROZEN OYSTER 8oz*40; Not for Retail Sale, Must be fully cooked before serving. Distributed by CJ Foods, Inc., Commerce, CA; 3) JAYONE FOODS, INC.) FROZEN OYSTER 8 oz*40, IQF, Distributed by Jayone Foods, Inc.., Paramount, CA 92723 Product of Korea

Class I - Dangerous
Recalled: June 8, 2012 Woosung America Other Foods

What Should You Do?

  1. Check if you have this product:
    1) Item number 3137810; 2) Item number 2237840; 3) Item number 36037800
  2. Do not eat it: Even if it looks and smells fine, do not consume this product.
  3. Throw it away or return it: You can return the product to the store for a full refund.
  4. Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
  5. Report problems: Report any issues to the FDA's Safety Reporting Portal.

⚠️ Emergency: If you experience severe symptoms after consuming this product, call 911 or Poison Control at 1-800-222-1222.

Recall Details

Company:
Woosung America Corp.
Reason for Recall:
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.
Classification:
Class I - Dangerous

Dangerous or defective products that predictably could cause serious health problems or death.

Status:
terminated

Product Information

Full Description:

Frozen Oysters: 1) CHORIPDONG) FROZEN OYSTER, IQF 8OZ*40; 2) CJ FOOD, INC.)FROZEN OYSTER 8oz*40; Not for Retail Sale, Must be fully cooked before serving. Distributed by CJ Foods, Inc., Commerce, CA; 3) JAYONE FOODS, INC.) FROZEN OYSTER 8 oz*40, IQF, Distributed by Jayone Foods, Inc.., Paramount, CA 92723 Product of Korea

Product Codes/Lot Numbers:

1) Item number 3137810; 2) Item number 2237840; 3) Item number 36037800

Distribution:

Distributed in: CA

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: F-1444-2012

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