Blueberry Crostata
Reason Egg wash is used on the product and is not listed on the ingredient list or allergen statement.
Sour Cherry Crostata recall
Recalled by Whole Foods Market · Emeryville, CA, United States
Class I — High risk. Reasonable probability of serious harm or death.
Why it was recalled
Egg wash is used on the product and is not listed on the ingredient list or allergen statement.
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
Sour Cherry Crostata, 1 pie Net. Wt. 1 lb. 6 oz (624 g) Whole Foods Market Inc., Emeryville, CA 94608
Quantity: ~110-120 units a week, both varieties. 19 weeks of production for ~2280 individual crostatas.
Food: Bread & bakery
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 units with sell by date prior to 8/14/13 and pack date prior to 8/10/13.
Where it was sold
California Nevada
FDA's distribution note: Northern CA and one location in NV
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
- Whole Foods Market
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Aug 10, 2013
- In FDA report of
- Sep 4, 2013
- Terminated
- Aug 29, 2013
- FDA recall number
- F-1856-2013 · event 66001
- 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.
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