Christ Kitchen *** Blameless Blondies*** recall
Recalled by Christ Kitchen · Spokane, WA, United States
Class I — High risk. Reasonable probability of serious harm or death.
Why it was recalled
Christ Kitchen is recalling Blameless Blondies, a dry bakery mix, because milk, soy and wheat allergens are not declared in product labeling.
Undeclared allergens: Milk Soy Wheat
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
The label reads in part "Christ Kitchen *** Blameless Blondies*** Net Weight: 15 oz (425gm). Product is a dry bakery mix and is packaged in a flexible plastic bag within a corrugated cardboard sleeve.
Quantity: Conflicting information provided by WSDA vs recalling firm. Firm states that 299 units have been distributed while WSDA states 375 units distribtued
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.
No lot codes. UPC 8 53143 00246 8
Where it was sold
Washington
FDA's distribution note: Spokane, WA
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 milk, soy, wheat; 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
- Christ Kitchen
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Jan 23, 2015
- In FDA report of
- Apr 8, 2015
- Terminated
- Mar 31, 2015
- FDA recall number
- F-1781-2015 · event 70454
- Official record
- FDA enforcement report search