Stumptown Cold Brew Coffee with Oat Milk Chocolate. Plant Based. Low Sugar. Made with Oatly! 11 Fl Oz. 325 ML. UPC 8 55186-00688 5. Sold in 12-count case UPC 10855186006882. Manufactured for Stumptown Coffee Roasters, 100 SE Salmon St. Portland, OR 97214

Class I - Dangerous
Recalled: July 22, 2022 Lyons Magnus Dairy & Eggs Nationwide

What Should You Do?

  1. Check if you have this product:
    Lot Code 6312 / Best By Date 12/12/2022. EXPANDED 8-10-2022 Lot Code 1802 / Best By Date 10/18/2022; Lot Code 2802 / Best By Date 10/19/2022; Lot Code 7202 / Best By Date 08/25/2022; Lot Code 8202 / Best By Date 08/26/2022
  2. Do not eat it: Even if it looks and smells fine, do not consume this product.
  3. Throw it away or return it: You can return the product to the store for a full refund.
  4. Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
  5. Report problems: Report any issues to the FDA's Safety Reporting Portal.

⚠️ Emergency: If you experience severe symptoms after consuming this product, call 911 or Poison Control at 1-800-222-1222.

Recall Details

Company:
Lyons Magnus, Inc
Reason for Recall:
Findings and potential for Cronobacter sakazakii and Clostridium botulinum.
Classification:
Class I - Dangerous

Dangerous or defective products that predictably could cause serious health problems or death.

Status:
terminated

Product Information

Full Description:

Stumptown Cold Brew Coffee with Oat Milk Chocolate. Plant Based. Low Sugar. Made with Oatly! 11 Fl Oz. 325 ML. UPC 8 55186-00688 5. Sold in 12-count case UPC 10855186006882. Manufactured for Stumptown Coffee Roasters, 100 SE Salmon St. Portland, OR 97214

Product Codes/Lot Numbers:

Lot Code 6312 / Best By Date 12/12/2022. EXPANDED 8-10-2022 Lot Code 1802 / Best By Date 10/18/2022; Lot Code 2802 / Best By Date 10/19/2022; Lot Code 7202 / Best By Date 08/25/2022; Lot Code 8202 / Best By Date 08/26/2022

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: F-1641-2022

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