CLASS I Food recall · Reported 16 Jan 2013 · FDA Enforcement Report
Kinnikinnick Pie Crust Gluten Free (frozen) weight Qty/Pkg recalled
United National Foods (Unfi) is recalling Kinnikinnick Pie Crust Gluten Free (frozen) weight Qty/Pkg: 2, distributed in California, Colorado, Texas, Washington. The recall was initiated on 28 Dec 2012 and the FDA has classified it as Class I.
Check your package
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
Recall details
- Recall number
- F-0865-2013
- FDA event ID
- 63998
- Recalling firm
- United National Foods (Unfi), Aurora, CO
- Brand
- Kinnikinnick
- Classification
- Class I
- Status
- Terminated
- Recall initiated
- 28 Dec 2012
- FDA classified
- 7 Jan 2013
- Reported
- 16 Jan 2013
- Type
- Voluntary: Firm initiated
- Customers notified by
- Letter
- Reason category
- Undeclared Egg
- Product category
- Cakes & Pastries
Timeline
| 28 Dec 2012 | Recall initiated by company | |
| 7 Jan 2013 | Classified by FDA | +10 days |
| 16 Jan 2013 | Published in enforcement report | +9 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
UNFI Aurora, Colorado is recalling certain Kinnikinnick Pie Crusts (frozen) because they were notified by the manufacturer, Kinnikinnick Foods (Alberta, Canada) that the products contain eggs and are not identified in the finished product labeling.
Product as listed by the FDA
Kinnikinnick Pie Crust Gluten Free (frozen) weight 290 g/ 10 oz Qty/Pkg: 2, UPC 620133006229, Kinnikinnick Foods 10940 120 Street, Edmonton, AB Canada.
Where it was distributed
Distributed to UNFI distribution centers located in WA, CA, CO, and TX.
Questions about this recall
Why was it recalled?
UNFI Aurora, Colorado is recalling certain Kinnikinnick Pie Crusts (frozen) because they were notified by the manufacturer, Kinnikinnick Foods (Alberta, Canada) that the products contain eggs and are not identified in the finished product labeling.
Which lots are affected?
US distribution: BB2013NO30; BB2013DE12; BB2013DE13; BB2013DE14; BB2013DE17; BB2013DE04; BB2013DE11; BB2013NO28; BB2013NO29; BB2013NO23; BB2013DE06; BB2013DE05; BB2013NO28; BB2013NO19; BB2013DE04; BB2013NO27.
Where was it sold?
Distributed to UNFI distribution centers located in WA, CA, CO, and TX.
What should I do if I have it?
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
What does Class I mean?
Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.
Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
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