Food Recall Check
Class I · High risk Terminated Initiated Sep 14, 2016 (10 years ago)

Field Day Organic Ranch Dressing packaged in an recall

Recalled by Drews LLC · Chester, VT, United States

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

Why it was recalled

Undeclared milk and egg allergen.

Undeclared allergens: Milk Egg

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

Field Day Organic Ranch Dressing packaged in an 8 fl. oz. glass bottle, UPC #042563600242. The lot code is located on the back of the bottle above the label. Specifically, the front label of the affected product is correctly labeled Field Day Organic Ranch Dressing, 8 fl oz. The issue is some bottles have an incorrect back label such that the contains statement does not list milk and egg as allergens. These bottles can be identified by UPC# 042563600259.

Quantity: N/A

Food: Sauces, dips & dressings

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 Code W210I, Best By date of Jan. 28, 2018

Where it was sold

Illinois

FDA's distribution note: IL

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, egg; 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
Drews LLC
Initiated by
Voluntary: Firm initiated
Recall initiated
Sep 14, 2016
In FDA report of
Dec 14, 2016
Terminated
Aug 15, 2017
FDA recall number
F-0677-2017 · event 75176
Official record
FDA enforcement report search

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