Food recall

Stumptown Coffee Corp recall: Stumptown Cold Brew Coffee and Chocolate with Oatmilk

Stumptown Coffee Corp, of Portland, OR, recalled Stumptown Cold Brew Coffee and Chocolate with Oatmilk. The FDA's reason: “Packaging failure that caused leakage.” The FDA classified it Class II: it could cause temporary or minor harm. The company began the recall voluntarily on June 5, 2020, and the FDA first listed it in its Enforcement Report of July 1, 2020. The FDA has closed the recall: it found the company did all it reasonably could to remove or correct the product.

How serious

Class II

It could cause temporary or minor harm

Why

Labeling, packaging or manufacturing problems

Status

Terminated

Closed August 18, 2020

The recall

Company
Stumptown Coffee Corp (Portland, OR)
Reason, in FDA's words
“Packaging failure that caused leakage.”
Where it was sold
distributed in CA,CO, NH, NY, OR, PA, TX, and WA.
Recall began
, by the company
FDA classified it
First in an FDA Enforcement Report
FDA event number
85817

The product recalled

As the FDA describes them, with the codes that tell whether a package is part of the recall.

  • F-1018-2020 Class II

    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.

    Codes: ***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.

    Quantity: 900 units

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Source and notes

U.S. Food and Drug Administration, Enforcement Reports (openFDA food recall data) (Public domain (U.S. government work); source U.S. Food and Drug Administration, openFDA), data as of July 1, 2020.

Each week the FDA lists the recalls it has classified in its Enforcement Report, often weeks after the company announced the recall, so a month with five weekly reports tends to count more. Each recall counts once, however many products it covers, in the month FDA first listed it. Class I means the food could cause serious harm or death, Class II temporary or minor harm, and Class III is unlikely to harm anyone. Meat, poultry and most egg products are recalled by the U.S. Department of Agriculture, not the FDA, and aren't included. For what to do with a recalled product, see the FDA's recalls page.