FDA recall record

Sid Wainer And Son Domaine de Provence La Cucina Tart Shells Produced Exclusively recall — FDA F-1613-2016

Product contains undeclared allergen, eggs.

Class Iclassification
F-1613-2016official record ID
Jul 13, 2016report date

Recall record at a glance

Official recordF-1613-2016
CategoryFood Recalls
ClassificationClass I
FDA record statusTerminated
Recalling firmSid Wainer And Son
Report dateJul 13, 2016
Recall initiation dateMay 27, 2016
Quantity117 cases (252 pieces box)
LocationNew Bedford, MA, United States

Official product description

Domaine de Provence La Cucina Tart Shells Produced Exclusively for Sid Wainer& Son, New Bedford, MA UPC Code: 708152149119 Item Number: 149110

Why the product was recalled

Product contains undeclared allergen, eggs.

Distribution information

AR, CT, DC, MA, ME, NC, NH, NJ, NY, PA, RI, TX,VT

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.

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