🔍 RecallPedia

ULTRA Fabric Reinforced Surgical Gown, X-Large, Sterile, Test File. The Kimberly-Clark ULTRA Fabric Reinforced Surgical Gown is a sterile, single use surgical gown intended to protect surgical patients and operating room personnel from the transfer of microorganisms, body fluids, and particulate material.

Class I - Dangerous
🏥 Medical Devices Recalled: December 31, 2010 Kimberly-Clark Diagnostic Equipment Nationwide

What Should You Do?

  1. Check if you have this product:
    Product Code: 95221-35, Unit Code: 90372
  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:
The impacted product was not intended for commercial distribution to end users.
Classification:
Class I - Dangerous

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

Status:
terminated

Product Information

Full Description:

ULTRA Fabric Reinforced Surgical Gown, X-Large, Sterile, Test File. The Kimberly-Clark ULTRA Fabric Reinforced Surgical Gown is a sterile, single use surgical gown intended to protect surgical patients and operating room personnel from the transfer of microorganisms, body fluids, and particulate material.

Product Codes/Lot Numbers:

Product Code: 95221-35, Unit Code: 90372

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-2425-2012

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