Hazelnut Cake Paradise Deli
Reason cake product is recalled due to undeclared soy lecithin. The canola spray oil containing soy lecithin was used but soy or soy lecithin is not declared on label.
Love Your Heart Cake recall
Recalled by Choice Northwest · Eugene, OR, United States
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Why it was recalled
cake product is recalled due to undeclared soy lecithin. The canola spray oil containing soy lecithin was used but soy or soy lecithin is not declared on label.
Undeclared allergen: Soy
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
Love Your Heart Cake, Paradise Deli brand, Net Wt. 14 oz., UPC 0 31619 40402 6. The label is read in parts: "***Contains: Fresh apples, fresh carrots, organic unbleached wheat flour, organic cane sugar, Oregon grown hazelnuts, raisins, cinnamon, baking soad, and baking powder***PARADISE DELI - PO Box 22411, Eugene, OR 97402 *** ".
Quantity: 48 counts
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.
Expiration date 5/12, 5/13, 5/20
Where it was sold
Oregon
FDA's distribution note: distributed in Oregon
Check the codes, then return or discard. Class II means eating it may cause temporary or reversible health problems. If your package matches the recalled codes, do not eat it - return it to the store or throw it away. The risk from an undeclared allergen is to people allergic to soy; 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
- Choice Northwest
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- May 5, 2017
- In FDA report of
- Jun 14, 2017
- Terminated
- Aug 15, 2017
- FDA recall number
- F-2328-2017 · event 77216
- 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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