Bix Produce Mixed Fruit products containing Cantaloupe recall

Recalled by FreshPoint Bix Produce Company, LLC · Little Canada, MN, United States

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

Why it was recalled

Potential Salmonella contamination.

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

Bix Produce Mixed Fruit products containing Cantaloupe, Honeydew, and Pineapple. Keep Refrigerated. Manufactured and Distributed by: Bix Produce Company, 3060 Centerville Road, Little Canada, MN 55117 Packaged with the following cuts and weights: 1. Item # 12192, Fruit, Chunk Mixed 1/2", 20 lb. 2. Item # 12240, Fruit, Chunk Mixed 5 lb. 3. Item # 12245, Fruit, Chunk Mixed 1" 20 lb.

Quantity: 44 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.

Lot number / Sales Order #: 1. P2760607-00, P2764334-00, P2765219-00, P2765878-00. 2. P2765875-00. 3. P2765892-00, P5221567-00.

Where it was sold

Iowa Minnesota North Dakota Wisconsin

FDA's distribution note: IA, MN, ND, WI

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: FreshPoint Bix Produce Company, LLC
Initiated by: Voluntary: Firm initiated
Recall initiated: Nov 17, 2023
In FDA report of: Dec 13, 2023
Terminated: Jan 15, 2025
FDA recall number: F-0670-2024 · event 93471
Official record: FDA enforcement report search

Also recalled with it (7 more products)

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

Class I · High risk Terminated Salmonella Nov 17, 2023