Food Recall Check
Class I · High risk Terminated Initiated Jan 3, 2014 (13 years ago)

Alaskan Birch Brittle with Dark Chocolate Biscotti-individually wrapped in cellophane recall

Recalled by Yukon Concessions Alaska LLC · Wasilla, AK, United States

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

Why it was recalled

Alaska Birch with Dark Chocolate Biscotti-individually wrapped is recalled due to undeclared wheat, soy, and milk.

Undeclared allergens: Milk Soy Wheat

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

Alaskan Birch Brittle with Dark Chocolate Biscotti-individually wrapped in cellophane. Product is sold under Tonia's Biscotti brand, net wt. 2 oz. Alaskan Birch Brittle Drizzled in dark chocolate-individually wrapped in cellophane. Product is sold under Tonia's Biscotti brand, net wt. 2 oz.

Quantity: unknown

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.

NONE

Where it was sold

Alaska

FDA's distribution note: distributed in Alaska only and products were sold on www.toniasbiscotti.com

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, soy, wheat; 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
Yukon Concessions Alaska LLC
Initiated by
Voluntary: Firm initiated
Recall initiated
Jan 3, 2014
In FDA report of
Mar 12, 2014
Terminated
May 13, 2014
FDA recall number
F-1617-2014 · event 67216
Official record
FDA enforcement report search

Also recalled with it (10 more products)

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