Blueberry Scones bulk packaged in cake boxes with parchment paper
Reason Undeclared soy lecithin and soybean oil on label
Marionberry Scones bulk packaged in cake boxes with parchment paper recall
Recalled by Skagit River Bakery & Cafe · Anacortes, WA, United States
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Why it was recalled
Undeclared soy lecithin and soybean oil 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
Marionberry Scones, bulk packaged in cake boxes with parchment paper, unwrapped. Products are not individual labeled and are held in bulk for retail sale. Each location has a notebook with all the ingredients used in the scones.
Quantity: estimated 1200 units
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.
None. Product has a date of delivery listed on invoice.
Where it was sold
Washington
FDA's distribution note: Distributed in WA.
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
- Skagit River Bakery & Cafe
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Aug 22, 2024
- In FDA report of
- Oct 2, 2024
- Terminated
- Sep 26, 2024
- FDA recall number
- F-1831-2024 · event 95253
- 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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