Kinnikinnick Gluten Free Original Homestyle Waffles Frozen… recall
Recalled by DPI Specialty Foods Northwest Inc. · Tualatin, OR, United States
Class I — High risk. Reasonable probability of serious harm or death.
Why it was recalled
DPI Specialty Foods NW is recalling Kinnikinnick Brand gluten free original homestyle waffles because they have the potential to contain the allergen milk, which is not declared on the label. Package contains a logo which indicates the product is dairy free.
Undeclared allergens: Milk 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
Kinnikinnick Gluten Free Original Homestyle Waffles Frozen Contains a logos on the package indicating it is gluten free, dairy free, and nut free. 210 g/7.4oz Qty/pkg - 6. UPC 62013300198 1. DPI item # 55844.
Quantity: 2220 cases
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.
20131209 and 20131231
Where it was sold
Oregon Washington
FDA's distribution note: WA and OR
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, 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
- DPI Specialty Foods Northwest Inc.
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Jan 13, 2014
- In FDA report of
- Feb 26, 2014
- Terminated
- Feb 21, 2014
- FDA recall number
- F-1535-2014 · event 67294
- Official record
- FDA enforcement report search