FDA recall record

Chicago Kimchee Korea chopped Kimchee packaged in 1 gallon, 1/2 gallon, 1/4 recall — FDA F-1096-2016

Undeclared anchovies in Kimchee product.

Class Iclassification
F-1096-2016official record ID
Apr 27, 2016report date

Recall record at a glance

Official recordF-1096-2016
CategoryFood Recalls
ClassificationClass I
FDA record statusTerminated
Recalling firmChicago Kimchee
Report dateApr 27, 2016
Recall initiation dateMar 10, 2016
Quantity1 gallon: 401 boxes, 4 jars/box 1/2 gallon: 167 boxes, 6 jars/box 1/4 gallon: 371 boxes, 12 jars/box 1/8 gallon: 113 boxes: 12 jars/box
LocationFranklin Park, IL, United States

Official product description

Korea chopped Kimchee packaged in 1 gallon, 1/2 gallon, 1/4 gallon, and 1/8 gallon packaged in glass jars inside plastic containers with multi colored label and black lettering.

Why the product was recalled

Undeclared anchovies in Kimchee product.

Distribution information

Products were distributed to several distributors in the chicagoland area.

How to read the classification

FDA Class I indicates a situation in which there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. The classification shown here comes directly from the FDA enforcement record.

Additional record details

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

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.