Domaine de Provence Neutral 3"¿ Cone Tart Shells Produced Exclusively for Sid Wainer & Son
Reason Product contains undeclared allergen, coconut.
Domaine de Provence La Cucina Tart Shells Produced Exclusively for Sid Wainer& Son recall
Recalled by Sid Wainer And Son · New Bedford, MA, United States
Class I — High risk. Reasonable probability of serious harm or death.
Why it was recalled
Product contains undeclared allergen, eggs.
Undeclared allergen: Egg
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
Domaine de Provence La Cucina Tart Shells Produced Exclusively for Sid Wainer& Son, New Bedford, MA UPC Code: 708152149119 Item Number: 149110
Quantity: 117 cases (252 pieces box)
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.
All product
Where it was sold
Arkansas Connecticut District of Columbia Massachusetts Maine North Carolina New Hampshire New Jersey New York Pennsylvania Rhode Island Texas Vermont
FDA's distribution note: AR, CT, DC, MA, ME, NC, NH, NJ, NY, PA, RI, TX,VT
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 egg; 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
- Sid Wainer And Son
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- May 27, 2016
- In FDA report of
- Jul 13, 2016
- Terminated
- Jan 19, 2017
- FDA recall number
- F-1613-2016 · event 74274
- 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.