Save to favorites
This feature is restricted to active members.
Join now to save favorites and get all member benefits, including over 1,400 reviews.
Join NowAlready a member? Sign in here.
Recalls & Warnings
ConsumerLab.com is keeping you informed with current product recalls and warnings.
Posted April 10, 2024
Powerade Variety Packs Recalled
Recalled Powerade drinks were distributed in South Carolina and Florida and are packaged in 20 oz PET bottles within a 24-variety pack. Eight bottles of Powerade Grape were also included in the variety packs. Recalled products can be further identified by the following:
- Powerade Zero Fruit Punch, Product Quantity: 149 cases, Lot Codes: 0013098209, 0013111742, 0013111657, 0013119902, Expiration Date: NOV1124AME
- Powerade Zero Mixed Berry, Product Quantity: 387 cases, Lot Codes: 0013098209, 0013111742, 0013111657, 0013119902, Expiration Date: NOV1124AMC
- Powerade Mountain Berry Blast, Product Quantity: 366 cases, Lot Codes: 0013098209, 0013111742, 0013111657, 0013119902, Expiration Date: NOV1124AMG and NOV18AMA
The Coca-Cola Company is notifying consignees or the public of the recall by email, letter, press release, telephone, or visit.
ConsumerLab tested a Powerade drink that is not included in the recall (Powerade Fruit Punch flavor 12 oz., which is different in both formula and product size) as part of its Review of Electrolytes & Sports Drinks.
For more information, use the links below.
FDA Enforcement Report: Powerade Zero Mixed Berry
FDA Enforcement Report: Powerade Zero Fruit Punch
FDA Enforcement Report: Powerade Mountain Berry Blast
See related recalls and warnings:
Jay Robb Protein Powder Recalled
Oregon’s Wild Harvest Warned by FDA for Manufacturing Violations
51 CBD Products Recalled Due to Lead Contamination
Turmeric Spice Recall Expanded to Include More Brands
Toxic Levels of Lead Found in Cinnamon Applesauce
Report a Problem
If you have experienced an unexpected and adverse reaction to a dietary supplement, nutritional product, or generic drug, we would like to hear about it, as we may investigate the problem. Please select from one of these options:
Dietary Supplement or Nutritional Product Problem Report
If you believe that a dietary supplement (e.g., vitamin, mineral, or herbal supplement) or other nutritional product has caused an unexpected, adverse reaction, we would like to know about it. We are collecting and organizing this information and may publish it. We might test the product in the future. You may also want to report the problem to the U.S. FDA through their Safety Reporting Portal at https://www.safetyreporting.hhs.gov.
Please complete the form below as accurately as possible. You may need to check the label on the product.
Thank you for submitting your report.
Generic Drug Problem Report
If you believe that a generic drug has not acted like the original drug, we would like to know about it. We are collecting and organizing this information and may publish it. We might test the product in the future. You may also want to report the problem to the U.S. FDA through their MedWatch program at the FDA MedWatch website.
Please complete the form below as accurately as possible. You may need to check the label on the drug.
Thank you for submitting your report.
