Food Recall Check
Class I · High risk Terminated Initiated Feb 26, 2014 (13 years ago)

Frozen Ice Cake recall

Recalled by Jin Sun Mi International INC · Los Angeles, CA, United States

Class I — High risk. Reasonable probability of serious harm or death.

Why it was recalled

Jin Sun Mi International is recalling watermelon ice bar product because it contains undeclared peanuts.

Undeclared allergen: Peanut

For someone with a food allergy the label is the only protection. An undeclared allergen can trigger a severe reaction even in a trace amount, which is why most of these recalls are Class I. All undeclared allergens recalls.

What was recalled

Frozen Ice Cake (Watermelon), 17.98 oz, 6 retail units/carton, UPC 8 801062 443055

Quantity: 194 units

Food: Fresh fruit Bread & bakery

Lot codes, dates and UPCs

A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.

Lot codes: 13.05.01F2 and 13.07.17F2 13.05.01F2 - This code date was printed on the retail units contained within Entry #EJA-5046135-1 (November) 13.07.17F2 - This code date was printed on the retail units contained within Entry #EJA-5045319-2 (October)

Where it was sold

California

FDA's distribution note: CA

Do not eat it. Class I means FDA judged there is a reasonable probability of serious illness or death. If the brand, size and lot or date code on your package match, throw the product away or return it to the store for a refund, and clean any surface or container it touched. If anyone has eaten it and feels unwell, contact a doctor and mention the recall. The risk from an undeclared allergen is to people allergic to peanut; for anyone else the product is generally not a safety concern. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.

Recalling firm
Jin Sun Mi International INC
Initiated by
Voluntary: Firm initiated
Recall initiated
Feb 26, 2014
In FDA report of
Apr 2, 2014
Terminated
Jun 12, 2014
FDA recall number
F-1689-2014 · event 67634
Official record
FDA enforcement report search

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