Food Recall Check
Class I · High risk Terminated Initiated Dec 22, 2017 (9 years ago)

Michelina's Fettuccine Alfredo recall

Recalled by Bellisio Foods Inc · Jackson, OH, United States

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

Why it was recalled

Undeclared soy. Firm was notified by a consumer that they found chicken in the product. The chicken contains soy.

Undeclared allergen: Soy

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

Michelina's Fettuccine Alfredo NET WT. 8.5 oz package Frozen CONTAINS MILK, WHEAT BELLISIO FOODS, INC., DULUTH, MN 55802 UPC 7 17854 10501 9

Quantity: 455 cs/12/8.5 oz packages - total: 5460 entrees

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 IDENTIFICATION CODE J7305D16 BEST BY 01NOV2018

Where it was sold

California Minnesota Ohio Texas Washington

FDA's distribution note: Product was shipped to CA, MN, OH, TX & WA.

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 soy; 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
Bellisio Foods Inc
Initiated by
Voluntary: Firm initiated
Recall initiated
Dec 22, 2017
In FDA report of
Jan 24, 2018
Terminated
Mar 21, 2018
FDA recall number
F-0569-2018 · event 78801
Official record
FDA enforcement report search