Simply Roundy's Natural Authentic Italian Butternut Squash Ravioli recall
Recalled by Roundys Supermarkets, Inc. · Oconomowoc, WI, United States
Class I — High risk. Reasonable probability of serious harm or death.
Why it was recalled
Roundy's is recalling Simply Roundy's Natural Authentic Italian Sweet Butternut Squash Ravioli because the product may contain undeclared cashew and almond. This product was manufactured and recalled by Bertagni 1882 SpA of Arcugnano, Italy due to undeclared cashews and almonds.
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
Simply Roundy's Natural Authentic Italian Butternut Squash Ravioli, Net Wt. 9 oz (255g). Packaged in a paper tray inside a plastic bag and wrapped around with paper band. Made in Italy. UPC 11150-50750
Quantity: 1542 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.
Lot Numbers: 506B, 508C, 511D, 512C, 513B, 516B, 520A, 522B, 522F, 523B, 523C, 529C, 530F, 531F, 535C, and 536A
Where it was sold
Illinois Wisconsin
FDA's distribution note: IL and WI only
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
- Roundys Supermarkets, Inc.
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Nov 18, 2015
- In FDA report of
- Mar 2, 2016
- Terminated
- Apr 11, 2016
- FDA recall number
- F-0633-2016 · event 72772
- Official record
- FDA enforcement report search