Food Recall Check
Class I · High risk Terminated Initiated Oct 5, 2020 (6 years ago)

Fresh From Meijer Triple Treat & Melon recall

Recalled by Meijer Inc./Traffic Dept. · Grand Rapids, MI, United States

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

Why it was recalled

potential risk of 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

FRESH FROM MEIJER TRIPLE TREAT & MELON, 22oz Clear plastic container, UPC 220453514736

Quantity: 13992 units

Food: Fresh fruit

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.

sold between Sept. 26 and Oct. 5 Oldest Best By date 10/8/2020

Where it was sold

Illinois Indiana Kentucky Michigan Ohio Wisconsin

FDA's distribution note: Meijer stores in Michigan, Ohio, Indiana, Illinois, Kentucky and Wisconsin.

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
Meijer Inc./Traffic Dept.
Initiated by
Voluntary: Firm initiated
Recall initiated
Oct 5, 2020
In FDA report of
Nov 18, 2020
Terminated
Nov 12, 2020
FDA recall number
F-0099-2021 · event 86561
Official record
FDA enforcement report search

Also recalled with it (11 more products)

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