Food Recall Check
Class I · High risk Terminated Initiated Feb 7, 2024 (3 years ago)

Marketside Bacon Ranch Crunch Chopped Salad Kit recall

Recalled by Braga Ranch INC. · Soledad, CA, United States

Class I — High risk. Reasonable probability of serious harm or death.

Why it was recalled

Product has the potential to be contaminated with Listeria monocytogenes.

Pathogen: Listeria

Listeria monocytogenes can grow even in the fridge and is especially dangerous in pregnancy.

The most serious food recalls: a contaminated product can cause outbreaks, hospitalisations and deaths, especially for pregnant people, young children, older adults and anyone with a weakened immune system. All bacteria & viruses recalls.

What was recalled

Marketside Bacon Ranch Crunch Chopped Salad Kit 12.76 oz. UPC 6 8113130544 0

Quantity: 1008 cases

Food: Leafy greens & salads

Lot codes, dates and UPCs

A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.

Lot: Lot codes starting with "BFFS" with Best By dates of 1/20/2024-2/19/2024 Best if Used By: 1/20/2024, 1/21/2024, 1/22/2024, 1/27/2024, 1/28/2024, 1/30/2024, 2/2/2024, 2/4/2024, 2/5/2024, 2/9/2024, 2/10/2024, 2/12/2024, 2/17/2024, 2/19/2024

Where it was sold

California

FDA's distribution note: U.S. distribution to the following: CA No foreign distribution.

Do not eat it. Class I means FDA judged there is a reasonable probability of serious illness or death. If the brand, size and lot or date code on your package match, throw the product away or return it to the store for a refund, and clean any surface or container it touched. If anyone has eaten it and feels unwell, contact a doctor and mention the recall. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.

Recalling firm
Braga Ranch INC.
Initiated by
Voluntary: Firm initiated
Recall initiated
Feb 7, 2024
In FDA report of
Mar 6, 2024
Terminated
Sep 4, 2024
FDA recall number
F-1008-2024 · event 93984
Official record
FDA enforcement report search

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