IQF Oysters 3lbs, Assi Brand, Item# 20083K,10x3 lb; Oyster Block, Assi Brand, item# 20085K, 30x1 lb; Oysters 8 oz - Tiny, Assi Brand, item# 20086, 40x8 oz; IQF Oysters 20 oz - Tiny, Assi Brand, item#20093, 20x20 oz.
Class I - DangerousWhat Should You Do?
- Check if you have this product: IQF Oysters 3lbs: UPC # 10081652200830, LOT # DO10921. Oyster Block: UPC # 10081652200854, LOT # DO10921. IQF Oysters 8 oz: UPC # 10081652200861, LOT # C-110304, DO11071. IQF Oysters 20 oz: UPC # 10081652200939, LOT # DO11021.
- Do not eat it: Even if it looks and smells fine, do not consume this product.
- Throw it away or return it: You can return the product to the store for a full refund.
- Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
- 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:
- KOREAN FARM, INC.
- Reason for Recall:
- Korean Farm is recalling Assi Brand Korean Oysters because they have been prepared, packed, or held under insanitary conditions whereby they may have become contaminated with filth, or whereby they 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:
IQF Oysters 3lbs, Assi Brand, Item# 20083K,10x3 lb; Oyster Block, Assi Brand, item# 20085K, 30x1 lb; Oysters 8 oz - Tiny, Assi Brand, item# 20086, 40x8 oz; IQF Oysters 20 oz - Tiny, Assi Brand, item#20093, 20x20 oz.
Product Codes/Lot Numbers:
IQF Oysters 3lbs: UPC # 10081652200830, LOT # DO10921. Oyster Block: UPC # 10081652200854, LOT # DO10921. IQF Oysters 8 oz: UPC # 10081652200861, LOT # C-110304, DO11071. IQF Oysters 20 oz: UPC # 10081652200939, LOT # DO11021.
Official Source
Always verify recall information with the official FDA source:
View on FDA.govFDA Recall Number: F-1742-2012
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