MRE Cookies & Cream Protein Shake. Whole Food Protein High protein shake. 11 FL OZ (325mL) Tetra Pak. UPC 8 10044-57389 3. 4-count case UPC 810044573961. Refrigerate after Opening. Distributed by: Redcon1, LLC, 701 Park of Commerce Blvd, Boca Raton, FL 33487

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 2112 / Best By Date 04/22/2023; Lot Code 3112 / Best By Date 04/23/2023; Lot Code 9612 / Best By Date 06/18/2023. EXPANDED 8-10-2022 Lot Code 5421 / Best By Date 09/02/2022 Lot Code 6421 / Best By Date 09/03/2022
  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:

MRE Cookies & Cream Protein Shake. Whole Food Protein High protein shake. 11 FL OZ (325mL) Tetra Pak. UPC 8 10044-57389 3. 4-count case UPC 810044573961. Refrigerate after Opening. Distributed by: Redcon1, LLC, 701 Park of Commerce Blvd, Boca Raton, FL 33487

Product Codes/Lot Numbers:

Lot Code 2112 / Best By Date 04/22/2023; Lot Code 3112 / Best By Date 04/23/2023; Lot Code 9612 / Best By Date 06/18/2023. EXPANDED 8-10-2022 Lot Code 5421 / Best By Date 09/02/2022 Lot Code 6421 / Best By Date 09/03/2022

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: F-1626-2022

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