Food Recall Check
Class II · Moderate risk Terminated Initiated Jun 1, 2016 (10 years ago)

Meadow Gold Dairy Pure Fresh Heavy Whipping Cream One Gallon recall

Recalled by Dean Foods, Inc. · Dallas, TX, United States

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

Insufficient pasteurization.

These are failures of the safety steps that keep food safe - cooking, pasteurising, keeping cold, sealing - even when no contaminant has yet been found. All processing & sanitation problems recalls.

What was recalled

Meadow Gold Dairy Pure Fresh Heavy Whipping Cream One Gallon (3.78L) in plastic one gallon container; Fresh Meadow Gold Dairy Pure Heavy Whipping Cream Half Pint (236 mL) in waxed cardboard carton; Meadow Gold Dairy Pure Fresh Heavy Whipping Cream One Quart (946mL) in waxed cardboard carton.

Quantity: 590 containers

Food: Milk & dairy

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.

1 gallon: 16-05 6-24-16 _ _:_ _ CK-D DL, UPC: 1570016615; Half pint: SELL BY 16-05 06-24-16 CK-D _ _:_ _ LK, UPC: 1570010018; Quart: SELL BY 16-05 06-24-16 CK-D _ _:_ _, UPC: 1570013210

Where it was sold

Idaho Oregon Utah Wyoming

FDA's distribution note: ID, OR, WY, UT

Check the codes, then return or discard. Class II means eating it may cause temporary or reversible health problems. If your package matches the recalled codes, do not eat it - return it to the store or throw it away. 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
Dean Foods, Inc.
Initiated by
Voluntary: Firm initiated
Recall initiated
Jun 1, 2016
In FDA report of
Oct 5, 2016
Terminated
Feb 16, 2017
FDA recall number
F-2604-2016 · event 74306
Official record
FDA enforcement report search

Also recalled with it (2 more products)

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

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