CLASS I Food recall · Reported 17 Oct 2018 · FDA Enforcement Report
Lic's Reese's Oreo recalled by Lloyd'S Ice Cream
Lloyd's Ice Cream is recalling Lic's Reese's Oreo, distributed in Indiana, Kentucky. The recall was initiated on 21 Sep 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-0027-2019
- FDA event ID
- 81111
- Recalling firm
- Lloyd's Ice Cream, Evansville, IN
- Brand
- Lic's Reese's
- Classification
- Class I
- Status
- Terminated
- Recall initiated
- 21 Sep 2018
- FDA classified
- 11 Oct 2018
- Reported
- 17 Oct 2018
- Type
- Voluntary: Firm initiated
- Customers notified by
- Telephone
- Reason category
- Undeclared Peanuts
- Product category
- Other
Timeline
| 21 Sep 2018 | Recall initiated by company | |
| 11 Oct 2018 | Classified by FDA | +20 days |
| 17 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
Lloyd s Ice Cream of Evansville, IN is voluntarily recalling pre-packed quarts of Reese s Oreo Ice Cream because the product label does not declare peanuts.
Product as listed by the FDA
Lic's REESE'S OREO, ONE QUART (946 mL), packed in Plastic quart container
Where it was distributed
Domestic Only: IN and KY
Questions about this recall
Why was it recalled?
Lloyd s Ice Cream of Evansville, IN is voluntarily recalling pre-packed quarts of Reese s Oreo Ice Cream because the product label does not declare peanuts.
Which lots are affected?
Manufactured: 4 /11 /2016 6/25/2018 Distributed Between: 4/12/16 9/17/18 Codes: 102,123,193,235,277,37,100,191,212,310,352,176
Where was it sold?
Domestic Only: IN and KY
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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