Food Recall Check
Class I · High risk Terminated Initiated Nov 17, 2015 (11 years ago)

Meijer frozen Butternut Squash Ravioli recall

Recalled by Bertagni 1882 · Arcugnano, N/A, Italy

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

Why it was recalled

Meijer frozen Butternut Squash Ravioli is recalled because product may contain undeclared cashew and almond.

Undeclared allergen: Tree nuts

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

Meijer frozen Butternut Squash Ravioli, product is packaged in a paper box, net weight 12 oz., UPC 760236398479

Quantity: 1080 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.

Expiration date: 11/5/2016 Lot code: 519 E

Where it was sold

California Illinois Indiana Kentucky Michigan Minnesota New York Ohio Oregon Wisconsin

FDA's distribution note: Bertagni product was distributed directly in CA, IL, MI, MN, NY, OH, and OR between 5/11/15 and 11/12/15. Meijer product was distributed in IL, IN, KY, MI, OH, and WI between 6/12/15 to 10/26/15.

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 tree nuts; 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
Bertagni 1882
Initiated by
Voluntary: Firm initiated
Recall initiated
Nov 17, 2015
In FDA report of
May 18, 2016
Terminated
Jan 23, 2017
FDA recall number
F-1044-2016 · event 72761
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.