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

Kinnikinnick Pancake & Waffle Mix -Weight recall

Recalled by Bozzutos' Inc. · Cheshire, CT, United States

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

Why it was recalled

Bozzutos Inc. is recalling Kinnikinnick Food's bakery products due to undeclared milk.

Undeclared allergen: Milk

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 Pancake & Waffle Mix -Weight: 454g/16 oz Cardboard Box UPC 62013310512 2

Quantity: 50 cases

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.

All lots up to and including Best Befor 2015JA06, 20150106, 150106

Where it was sold

Massachusetts Maine New Hampshire New Jersey New York Rhode Island

FDA's distribution note: Ct, MA, ME, NH, NJ, NY, RI

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 milk; 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
Bozzutos' Inc.
Initiated by
Voluntary: Firm initiated
Recall initiated
Jan 13, 2014
In FDA report of
Mar 5, 2014
Terminated
Mar 22, 2016
FDA recall number
F-1554-2014 · event 67355
Official record
FDA enforcement report search

Also recalled with it (1 more product)

FDA files each product of one recall action separately; these share the same FDA event.