FDA recall record

Cheesewich Factory RTE bacon and eggs 3.6 oz package recall — FDA F-0515-2020

Eggs in RTE bacon and egg packet may contain Listeria Monocytogenes.

Class Iclassification
F-0515-2020official record ID
Jan 22, 2020report date

Recall record at a glance

Official recordF-0515-2020
CategoryFood Recalls
ClassificationClass I
FDA record statusTerminated
Recalling firmCheesewich Factory
Report dateJan 22, 2020
Recall initiation dateDec 27, 2019
Quantity2516 cases, 6793.2 lbs.
LocationHodgkins, IL, United States

Official product description

RTE bacon and eggs 3.6 oz package

Why the product was recalled

Eggs in RTE bacon and egg packet may contain Listeria Monocytogenes.

Distribution information

The firm distributed product to 4 distribution centers, Dot Foods, IL, S. Abrahams, MI, KINEX, NC, and Lipari Foods, MI.

How to read the classification

FDA Class I indicates a situation in which there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. The classification shown here comes directly from the FDA enforcement record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

FDA source limitation: openFDA enforcement reports are a reference dataset, not a live public-alert or recall-lifecycle service. FDA notes that enforcement-report status may not be updated after classification. Confirm current actions with the FDA, recalling firm or appropriate healthcare professional when relevant.