Food Recall Check
Class I · High risk Terminated Initiated Jul 18, 2012 (14 years ago)

Wellements Baby Move Prune Concentrate with Prebiotics recall

Recalled by Wellements, LLC · Scottsdale, AZ, United States

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

Why it was recalled

Wellements is recalling Wellements Baby Move Prune Concentrate, 4oz. because they have confirmed that their supplier of the ingredient galacto-oligosaccharide which is used in the Baby Move product may be contaminated 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

Wellements Baby Move Prune Concentrate with Prebiotics, 4oz., 12 units per case, SKU# 141161, UPC 729609019878.

Quantity: 66,965 units

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# 12009, 12025, 12137, 12174, 12177, 12178, and 12179.

Where it was sold

Nationwide.

FDA's distribution note: Nationwide and Canada

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
Wellements, LLC
Initiated by
Voluntary: Firm initiated
Recall initiated
Jul 18, 2012
In FDA report of
Aug 1, 2012
Terminated
Nov 29, 2012
FDA recall number
F-1799-2012 · event 62615
Official record
FDA enforcement report search

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