Food Recall Check
Class I · High risk Terminated Initiated Aug 6, 2012 (14 years ago)

Menno Beachy Cresco recall

Recalled by Menno Beachy · Cresco, IA, United States

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

Why it was recalled

Salmonella Montevideo was isolated in one lot of the grape tomatoes

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

Menno Beachy, Cresco, IA Certified Organic Grape Tomato packaged in 1-pint square-shaped clear plastic clamshell containers, UPC 044419310176, 12/1-pint. containers per case.

Quantity: 20/12/1-pt. container cases

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 numbers MB725GT0, MB725GT3, and MB725GT8. These lot numbers only appear on the case label, not on the clamshell label.

Where it was sold

Michigan Minnesota Wisconsin

FDA's distribution note: Distribution was made to a food distributor in MN who further distributed the product to retail stores located in MN, WI, and MI.

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
Menno Beachy
Initiated by
Voluntary: Firm initiated
Recall initiated
Aug 6, 2012
In FDA report of
Aug 29, 2012
Terminated
Oct 26, 2012
FDA recall number
F-1992-2012 · event 62793
Official record
FDA enforcement report search