Food Recall Check
Class II · Moderate risk Terminated Initiated Sep 18, 2018 (8 years ago)

Oregon Heritage Farms Family Blend Apple Cider recall

Recalled by Oregon Heritage Developments Inc dba Oregon Heritage Farms · Beaverton, OR, United States

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

Why it was recalled

Oregon Heritage Farms Family Blend Apple Cider, 1 gallon size, is recalled due to elevated level of patulin.

Some of these cause harm only with repeated exposure (lead in spices, for example), others act within hours (histamine poisoning from spoiled fish). All chemical contamination recalls.

What was recalled

Oregon Heritage Farms Family Blend Apple Cider, 100% Juice, 1 gallon plastic container, UPC: 8 53581 00202 0. The label is read in parts: "***FAMILY BLEND Apple Cider 100% Juice Not from concentrate *** Pasteurized ***Refrigerate After Opening *** Ingredients: Apple Cider ***Pressed, Bottled, and Distributed: Oregon Heritage Farms 22801 SW Scholls Ferry Road Hillsboro, OR 97123 ***".

Quantity: 1632 cases (6528/1 gal. containers or 6,528 gallons total)

Food: Fresh fruit Juice & beverages

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 codes on bottle: 227OHF18 231OHF18 225OHF18

Where it was sold

Oregon

FDA's distribution note: distributed in OR.

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
Oregon Heritage Developments Inc dba Oregon Heritage Farms
Initiated by
Voluntary: Firm initiated
Recall initiated
Sep 18, 2018
In FDA report of
Oct 10, 2018
Terminated
Oct 12, 2018
FDA recall number
F-0006-2019 · event 81062
Official record
FDA enforcement report search

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