Check the Batch
Class IITerminated in FDA datasetRecall initiated Jun 14, 2012

IQF Oysters 3lbs, Assi Brand, Item# 20083K,10x3 lb; Oyster Block, Assi Brand, item# 20085K,…

Recalling firm: KOREAN FARM, INC.

Why it was recalled

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…

Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: Mar 8, 2013.

Check your package

Compare the exact product and package details with the label you have.

ProductIQF 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.
Package size3lbs

FDA code information

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.

Match the product, package size, and code together. A missing match does not guarantee safety.

Full FDA record and distribution details

Original product 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.

Extracted codes and context

TypeCode / valueContext
lotC-110304 10081652200854, LOT # DO10921. IQF Oysters 8 oz: UPC # 10081652200861, LOT # C-110304, DO11071. IQF Oysters 20 oz: UPC # 10081652200939, LOT # DO11021.

Original FDA recall reason

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.

Recall details

Recall number
F-1742-2012
Event ID
51667
FDA status
Terminated
Initiated
Jun 14, 2012
Reported
Jul 18, 2012
Classified
Jul 10, 2012
Terminated
Mar 8, 2013
Quantity
638 cartons
Location
Santa Fe Springs, CA, United States
Initiation type
Voluntary: Firm initiated
Notification
Letter

Where it was distributed

Nationwide in the US.

FDA source record · F-1742-2012

Data updated September 16, 2026. View official FDA data ↗

Follow official FDA and manufacturer guidance.