CLASS I Food recall · Reported 7 Oct 2015 · FDA Enforcement Report
Caramel Caribou Ice Cream, frozen in bulk round container recalled
The Ice Cream Club is recalling Caramel Caribou Ice Cream, frozen in bulk round container, distributed nationwide in the US. The recall was initiated on 31 Aug 2015 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-3251-2015
- FDA event ID
- 72088
- Recalling firm
- The Ice Cream Club, Boynton Beach, FL
- Brand
- Caramel Caribou
- Classification
- Class I
- Status
- Terminated
- Recall initiated
- 31 Aug 2015
- FDA classified
- 28 Sep 2015
- Reported
- 7 Oct 2015
- Type
- Voluntary: Firm initiated
- Customers notified by
- Telephone
- Reason category
- Undeclared Peanuts
- Product category
- Ice Cream & Frozen Desserts
Timeline
| 31 Aug 2015 | Recall initiated by company | |
| 28 Sep 2015 | Classified by FDA | +28 days |
| 7 Oct 2015 | 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
Product contains undeclared peanuts
Product as listed by the FDA
Caramel Caribou Ice Cream, 3 gal, frozen in bulk round container.
Where it was distributed
Nationwide to retail dipping stores, retirement communities, and one distributor: FL, GA, AL, TX, SC, RI, MI
Nationwide AlabamaFloridaGeorgiaMichiganRhode IslandSouth CarolinaTexas
Questions about this recall
Why was it recalled?
Product contains undeclared peanuts
Which lots are affected?
Lot 5333. No exp date indicated by firm
Where was it sold?
Nationwide to retail dipping stores, retirement communities, and one distributor: FL, GA, AL, TX, SC, RI, MI
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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