CLASS I Food recall · Reported 2 Jan 2013 · FDA Enforcement Report
CMC Pumpkin Coffee Cake recalled by Golub
Golub is recalling CMC Pumpkin Coffee Cake, distributed in Massachusetts. The recall was initiated on 21 Oct 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-0852-2013
- FDA event ID
- 63697
- Recalling firm
- Golub, Schenectady, NY
- Brand
- CMC Pumpkin
- Classification
- Class I
- Status
- Terminated
- Recall initiated
- 21 Oct 2012
- FDA classified
- 21 Dec 2012
- Reported
- 2 Jan 2013
- Type
- Voluntary: Firm initiated
- Customers notified by
- Press Release
- Reason category
- Labeling Errors
- Product category
- Cakes & Pastries
Timeline
| 21 Oct 2012 | Recall initiated by company | |
| 21 Dec 2012 | Classified by FDA | +61 days |
| 2 Jan 2013 | Published in enforcement report | +12 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
CMC Cinnamon Coffee Cake was incorrectly labeled as Pumpkin Coffee Cake and therefore did not list walnuts as an ingredient
Product as listed by the FDA
CMC Pumpkin Coffee Cake 16 oz UPC: 041735225726 Price Chopper/Box
Where it was distributed
Worcester, MA
Questions about this recall
Why was it recalled?
CMC Cinnamon Coffee Cake was incorrectly labeled as Pumpkin Coffee Cake and therefore did not list walnuts as an ingredient
Which lots are affected?
UPC # 41735-225726 expiration date between October 17 and October 25, 2012
Where was it sold?
Worcester, MA
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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