CLASS II Food recall · Reported 17 Aug 2016 · FDA Enforcement Report
Sundae Shoppe Novelty Ice Cream Dipped "Variety"cones recalled
Mister Cookie Face is recalling Sundae Shoppe Novelty Ice Cream Dipped "Variety"cones, distributed in Illinois, North Carolina, Ohio. The recall was initiated on 30 Jun 2016 and the FDA has classified it as Class II.
Recall details
- Recall number
- F-1915-2016
- FDA event ID
- 74597
- Recalling firm
- Mister Cookie Face, Lakewood, NJ
- Brand
- Sundae Shoppe
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- 30 Jun 2016
- FDA classified
- 6 Aug 2016
- Reported
- 17 Aug 2016
- Type
- Voluntary: Firm initiated
- Customers notified by
- Press Release
- Reason category
- Undeclared Peanuts
- Product category
- Ice Cream & Frozen Desserts
Timeline
| 30 Jun 2016 | Recall initiated by company | |
| 6 Aug 2016 | Classified by FDA | +37 days |
| 17 Aug 2016 | Published in enforcement report | +11 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Sundae Shoppe Novelty Ice Cream Dipped "Variety" Ice Cream Cones are being recalled because they may contain peanuts which are not declared on the allergen statement.
Product as listed by the FDA
Sundae Shoppe Novelty Ice Cream Dipped "Variety"cones, 32 oz. box, Manufactured by Mister Cookie Face LLC, Lakeland, NJ and Distributed by Aldi, Batavia, IL 60510, UPC 041498191962
Where it was distributed
IL, NC and OH
Stores named: Aldi
Questions about this recall
Why was it recalled?
Sundae Shoppe Novelty Ice Cream Dipped "Variety" Ice Cream Cones are being recalled because they may contain peanuts which are not declared on the allergen statement.
Where was it sold?
IL, NC and OH
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 II mean?
Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.
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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