Food Recall Check
Class I · High risk Terminated Initiated Jun 15, 2017 (9 years ago)

DFS Cranberry Pumpkin Salad recall

Recalled by Morski Brands Inc. dba Dawn's Fresh Foods · Portage, WI, United States

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

Why it was recalled

Cranberry Pumpkin Salad prepared with pumpkin seeds that might be contaminated with Listeria monocytogenes.

Pathogen: Listeria

Listeria monocytogenes can grow even in the fridge and is especially dangerous in pregnancy.

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

DFS Cranberry Pumpkin Salad. Contains 4 / 8 Lb Bags, Net WT 32 lbs Item # 12071, Manufactured for Direct Food Service by Dawns Foods - Portage, WI.

Quantity: 4284 cases (4 / 8# bags per case)

Food: Berries

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 No.: - Exp date 1147 - 4/24/18 1157  4/25/18 1167  4/26/18 1177  4/27/18 1187  4/28/18 1197  4/29/18 1217  5/01/18 1237  5/03/18 1287  5/09/18 1307  5/10/18 1337  5/13/18 1357  5/15/18 1407  5/20/18 1447  5/24/18 1457  5/25/18 1517  5/31/18 1527  6/01/18 1537  6/02/18 1547  6/03/18

Where it was sold

FDA's distribution note: Ill

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
Morski Brands Inc. dba Dawn's Fresh Foods
Initiated by
Voluntary: Firm initiated
Recall initiated
Jun 15, 2017
In FDA report of
Aug 2, 2017
Terminated
Sep 8, 2017
FDA recall number
F-2947-2017 · event 77675
Official record
FDA enforcement report search

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