CLASS I Food recall · Reported 24 Oct 2018 · FDA Enforcement Report
Sweet Me Creamery Brookie Dough ice cream recalled by Kemps
Kemps is recalling Sweet Me Creamery Brookie Dough ice cream, distributed in Illinois, Minnesota, North Dakota, Wisconsin. The recall was initiated on 8 Oct 2018 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-0050-2019
- FDA event ID
- 81216
- Recalling firm
- Kemps, Falcon Heights, MN
- Classification
- Class I
- Status
- Terminated
- Recall initiated
- 8 Oct 2018
- FDA classified
- 18 Oct 2018
- Reported
- 24 Oct 2018
- Type
- Voluntary: Firm initiated
- Customers notified by
- Telephone
- Reason category
- Undeclared Peanuts
- Product category
- Ice Cream & Frozen Desserts
Timeline
| 8 Oct 2018 | Recall initiated by company | |
| 18 Oct 2018 | Classified by FDA | +10 days |
| 24 Oct 2018 | Published in enforcement report | +6 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Sweet Me Creamery Brookie Dough ice cream may contain undeclared peanuts.
Product as listed by the FDA
Sweet Me Creamery Brookie Dough ice cream, packaged in following configuration: 1 Pint (473 ML), UPC: 41483-04219 or 4-Pack of 1 Pint (473 ML) containers Net Half Gallon (1.89L), UPC 41483-04241. Vanilla ice cream swirled with sea salt fudge and pieces of cookie dough and brownies.
Where it was distributed
IL, MN, ND, WI
Questions about this recall
Why was it recalled?
Sweet Me Creamery Brookie Dough ice cream may contain undeclared peanuts.
Which lots are affected?
Best By: DEC 4 2019, DEC 5 2019, DEC 13 2019, FEB 15 2020, FEB 16 2020
Where was it sold?
IL, MN, ND, WI
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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