Food Recall Check
Class I · High risk Terminated Initiated Feb 15, 2017 (10 years ago)

Ditos Heart shaped plastic platter of mixed fruits with Dip of… recall

Recalled by Dito's - A Sysco Company · Anchorage, AK, United States

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

Why it was recalled

Mixed fruits with Dip of Chocolate Frosting platters are recalled due to undeclared milk and soy

Undeclared allergens: Milk Soy

For someone with a food allergy the label is the only protection. An undeclared allergen can trigger a severe reaction even in a trace amount, which is why most of these recalls are Class I. All undeclared allergens recalls.

What was recalled

Ditos Heart shaped plastic platter of mixed fruits with Dip of Chocolate Frosting- Refrigerated. Net wt. 40 oz. UPC 8 93268 00198 4. The label is read in parts: "***Heart Platter Mixed Fruit w/ Dip***40 oz.*** Cantaloupe (US), Honeneydew (Mexico), Pineapple (Costa Rica)***by Dito's LLC, Anchorage, AK 99518***".

Quantity: 30 cases (4 platters per case)

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.

use by date: 02/14/2017, 02/15/2017, 02/16/2017, and 02/19/2017.

Where it was sold

Alaska

FDA's distribution note: in AK only

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. The risk from an undeclared allergen is to people allergic to milk, soy; for anyone else the product is generally not a safety concern. 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
Dito's - A Sysco Company
Initiated by
Voluntary: Firm initiated
Recall initiated
Feb 15, 2017
In FDA report of
Mar 29, 2017
Terminated
Apr 13, 2017
FDA recall number
F-1629-2017 · event 76510
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.