Recall record at a glance
| Official record | F-1044-2016 |
|---|---|
| Category | Food Recalls |
| Classification | Class I |
| FDA record status | Terminated |
| Recalling firm | Bertagni 1882 |
| Report date | May 18, 2016 |
| Recall initiation date | Nov 17, 2015 |
| Quantity | 1080 cases |
| Location | Arcugnano, N/A, Italy |
Official product description
Meijer frozen Butternut Squash Ravioli, product is packaged in a paper box, net weight 12 oz., UPC 760236398479
Why the product was recalled
Meijer frozen Butternut Squash Ravioli is recalled because product may contain undeclared cashew and almond.
Distribution information
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.
How to read the classification
FDA Class I indicates a situation in which there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. The classification shown here comes directly from the FDA enforcement record.
Additional record details
Recall type: Voluntary: Firm initiated. Initial notification: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit.
What to do next
If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.
About this record
Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.
FDA source limitation: openFDA enforcement reports are a reference dataset, not a live public-alert or recall-lifecycle service. FDA notes that enforcement-report status may not be updated after classification. Confirm current actions with the FDA, recalling firm or appropriate healthcare professional when relevant.