🔍 RecallPedia

U by Kotex¿ Sleek¿, Regular/Super Tampons, 34 Count Multipack

Class I - Dangerous
🏥 Medical Devices Recalled: December 11, 2018 Kimberly-Clark Other Medical Devices Nationwide

What Should You Do?

  1. Check if you have this product:
    Package UPC: 36000426663; Case UPC: 10036000426660; Lot Numbers: NN629401B, NN629501A, NN631301B, NN631401A, NN631401B, NN632213A, NN632213B, NN703113B, NN703213A, NN705513D, NN706513A, NN706513B, NN706613A, NN706613B, NN708713A, NN708713B, NN711413A, NN711413B, NN713113A, NN713113B, NN713213C, NN713213D, NN714513B, NN714613C, NN716613A, NN719413B, NN719513C, NN720613B, NN720713A, NN724713B, NN724813A, NN726813A, NN726813B, NN726913A, NN728313A, NN728313B, NN729713A, NN729713B, NN730913C, NN730913D, NN732613B, NN733813B, NN733913A, NN735313A, NN735313B, NN801413D, NN801513A, NN802913A, NN804313A, NN804313B, NN805713B, NN805813A, NN809913B, NN811213D, NN812613D, NN812713A, NN814013C, NN814013D, NN815513A, NN816813D, NN816913A, NN819613C, NN819613D, NN822513A, NN822513B, NN826613C, NN826613D, NN826713A.
  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:
Kimberly-Clark Corporation
Reason for Recall:
Potential for tampon to come apart upon removal.
Classification:
Class I - Dangerous

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

Status:
terminated

Product Information

Full Description:

U by Kotex¿ Sleek¿, Regular/Super Tampons, 34 Count Multipack

Product Codes/Lot Numbers:

Package UPC: 36000426663; Case UPC: 10036000426660; Lot Numbers: NN629401B, NN629501A, NN631301B, NN631401A, NN631401B, NN632213A, NN632213B, NN703113B, NN703213A, NN705513D, NN706513A, NN706513B, NN706613A, NN706613B, NN708713A, NN708713B, NN711413A, NN711413B, NN713113A, NN713113B, NN713213C, NN713213D, NN714513B, NN714613C, NN716613A, NN719413B, NN719513C, NN720613B, NN720713A, NN724713B, NN724813A, NN726813A, NN726813B, NN726913A, NN728313A, NN728313B, NN729713A, NN729713B, NN730913C, NN730913D, NN732613B, NN733813B, NN733913A, NN735313A, NN735313B, NN801413D, NN801513A, NN802913A, NN804313A, NN804313B, NN805713B, NN805813A, NN809913B, NN811213D, NN812613D, NN812713A, NN814013C, NN814013D, NN815513A, NN816813D, NN816913A, NN819613C, NN819613D, NN822513A, NN822513B, NN826613C, NN826613D, NN826713A.

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-0750-2019

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