Food Recall Check
Class II · Moderate risk Terminated Initiated Jun 5, 2020 (6 years ago)

Stumptown Cold Brew Coffee and Chocolate with Oatmilk recall

Recalled by Stumptown Coffee Corp · Portland, OR, United States

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

Why it was recalled

Packaging failure that caused leakage.

See the recall's own reason text for the specifics. All other reasons recalls.

What was recalled

Stumptown Cold Brew Coffee and Chocolate with Oatmilk. Product is TetraPak Prisma Pak aseptic packaging. Keep refrigerated. Net 11 fl. oz (325 mL). UPC on the single unit is 8 55186 00688 5.

Quantity: 900 units

Food: Chocolate & candy 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.

***THE SINGLE UNIT HAS THE FOLLOWING CODE: 12OCT20 3700-02 55-446 8:35 - 9:01. ***THE MASTER CASE HAS THE FOLLOWING CODE: 12 OCT 2020 3700-02. The lot code breaks down as follows: -Expiration dates or best-by date: October 12, 2020. -Julian date (reversed) 3700: 073 2020 (03/13/20) -Filling line: 02 -Product ID: 55-446 -Timestamp range: 8:35 - 9:01. Each single unit is stamped with a time that the product was filled.

Where it was sold

California Colorado New Hampshire New York Oregon Pennsylvania Texas Washington

FDA's distribution note: distributed in CA,CO, NH, NY, OR, PA, TX, and WA.

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
Stumptown Coffee Corp
Initiated by
Voluntary: Firm initiated
Recall initiated
Jun 5, 2020
In FDA report of
Jul 1, 2020
Terminated
Aug 18, 2020
FDA recall number
F-1018-2020 · event 85817
Official record
FDA enforcement report search

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