CLASS I Food recall · Reported 22 Jan 2020 · FDA Enforcement Report
RTE bacon and eggs package recalled by Cheesewich Factory
Cheesewich Factory is recalling RTE bacon and eggs package, distributed in Illinois, Michigan, North Carolina. The recall was initiated on 27 Dec 2019 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-0515-2020
- FDA event ID
- 84641
- Recalling firm
- Cheesewich Factory, Hodgkins, IL
- Brand
- Rte
- Classification
- Class I
- Status
- Terminated
- Recall initiated
- 27 Dec 2019
- FDA classified
- 16 Jan 2020
- Reported
- 22 Jan 2020
- Type
- Voluntary: Firm initiated
- Customers notified by
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Reason category
- Listeria
- Product category
- Eggs
Timeline
| 27 Dec 2019 | Recall initiated by company | |
| 16 Jan 2020 | Classified by FDA | +20 days |
| 22 Jan 2020 | 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
Eggs in RTE bacon and egg packet may contain 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
RTE bacon and eggs 3.6 oz package
Where it was distributed
The firm distributed product to 4 distribution centers, Dot Foods, IL, S. Abrahams, MI, KINEX, NC, and Lipari Foods, MI.
Questions about this recall
Is RTE bacon and eggs package recalled?
Yes. Cheesewich Factory recalled RTE bacon and eggs package on 27 Dec 2019. The recall is Class I and its status is Terminated. Recall number F-0515-2020.
Why was it recalled?
Eggs in RTE bacon and egg packet may contain Listeria Monocytogenes.
Which lots are affected?
USE BY" dates 12/27/19, 1/3/20, 1/23/20, 1/30/20, 2/6/20, 2/14/20, 2/19/20 and 2/28/20 and lot codes 281191, 302191, 309191, 316191, 323191, 331191, 336191, 344191
Where was it sold?
The firm distributed product to 4 distribution centers, Dot Foods, IL, S. Abrahams, MI, KINEX, NC, and Lipari Foods, 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 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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