CLASS I Food recall · Reported 4 Oct 2023 · FDA Enforcement Report
Mini Roll Cake Assorted recalled by Ice Cream House
Ice Cream House is recalling Mini Roll Cake Assorted, distributed in New Jersey, New York, Ohio. The recall was initiated on 22 Aug 2023 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-1676-2023
- FDA event ID
- 92966
- Recalling firm
- Ice Cream House, Brooklyn, NY
- Classification
- Class I
- Status
- Terminated
- Recall initiated
- 22 Aug 2023
- FDA classified
- 28 Sep 2023
- Reported
- 4 Oct 2023
- Type
- Voluntary: Firm initiated
- Customers notified by
- Telephone
- Reason category
- Listeria
- Product category
- Bread
Timeline
| 22 Aug 2023 | Recall initiated by company | |
| 28 Sep 2023 | Classified by FDA | +37 days |
| 4 Oct 2023 | 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
Products may be contaminated with Listeria monocytogenes.
Listeria monocytogenes can grow at refrigerator temperatures. Infection is most dangerous for pregnant women, newborns, older adults and people with weakened immune systems. Symptoms can appear up to 70 days after eating contaminated food.
Product as listed by the FDA
Mini Roll Cake Assorted; parve; 8 PACK / SINGLE; UPC: 0-91404-15350-8
Where it was distributed
OH, NJ, NY
Questions about this recall
Is Mini Roll Cake Assorted recalled?
Yes. Ice Cream House recalled Mini Roll Cake Assorted on 22 Aug 2023. The recall is Class I and its status is Terminated. Recall number F-1676-2023.
Why was it recalled?
Products may be contaminated with Listeria monocytogenes.
Which lots are affected?
No codes.
Where was it sold?
OH, NJ, NY
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 21 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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|---|---|---|---|---|---|
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