Food Recall Check
Class I · High risk Terminated Initiated Dec 31, 2012 (14 years ago)

Kinnikinnick Foods Brand Frozen Pie Crusts recall

Recalled by Jerusalem Manufacturing Natural Foods & Wholesalers, Inc. · Dearborn, MI, United States

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

Why it was recalled

Kinnikinnick Foods Inc., a Canadian manufacturer notifed Jerusalem Manufacturing Natural Food and Wholesalers, Inc. in Dearborn, MI to recall the Kinnikinnick Foods Brand Frozen Pies, 290g/10 ounces. 2 crusts per box, 6 boxes per case due to EGG not declared on the label.

Undeclared allergen: Egg

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

Kinnikinnick Foods Brand Frozen Pie Crusts, 290g/10 ounces. 2 crusts per box, 6 boxes per case

Quantity: 80 cs

Food: 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.

Product code 620133006009 and lot BB2013DE13

Where it was sold

Michigan

FDA's distribution note: MI Only (Dexter and Clinton Twp)

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 egg; 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
Jerusalem Manufacturing Natural Foods & Wholesalers, Inc.
Initiated by
Voluntary: Firm initiated
Recall initiated
Dec 31, 2012
In FDA report of
Feb 6, 2013
Terminated
Feb 7, 2013
FDA recall number
F-0948-2013 · event 63996
Official record
FDA enforcement report search

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