Food Recall Check
Class I · High risk Terminated Initiated Sep 12, 2014 (12 years ago)

2-5 lb recall

Recalled by Boskovich Farms, Inc · Oxnard, CA, United States

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

Why it was recalled

Boskovich Farms is recalling Roma Tomatoes because they may be contaminated with Salmonella.

Pathogen: Salmonella

Salmonella is the most common cause of food recalls for bacteria, often in eggs, produce, nuts and spices.

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

2-5 lb. clear plastic overwrapped black poly trays of 3/8" diced Roma Tomato per cardboard carton. Cardboard carton labeled: 2-5 LB. DICED TOMATOES 3/8  PACKED BY BOSKOVICH FARMS OXNARD CA, 93030 PRODUCT OF MEXICO.

Quantity: 12 units

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.

L091-EI03712, L091-EI09362.

Where it was sold

California

FDA's distribution note: CA

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
Boskovich Farms, Inc
Initiated by
Voluntary: Firm initiated
Recall initiated
Sep 12, 2014
In FDA report of
Oct 8, 2014
Terminated
Nov 14, 2014
FDA recall number
F-2535-2014 · event 69267
Official record
FDA enforcement report search

Also recalled with it (1 more product)

FDA files each product of one recall action separately; these share the same FDA event.