Class II — Potential Health Hazard

Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.

ULTRA Fabric Reinforced surgical Gown X-Large Sterile The product is Recalled by Kimberly-Clark Corporation Due to Package seam of some units may not remain...

Date: July 5, 2012
Company: Kimberly-Clark Corporation
Status: Terminated
Source: FDA (Device)

What You Should Do

Stop using this product immediately. Do not consume, use, or distribute it.

Return the product to the place of purchase for a full refund. If you have questions, contact Kimberly-Clark Corporation directly.

Affected Products

ULTRA Fabric Reinforced surgical Gown X-Large Sterile The product 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.

Quantity: 89,856 (28 units per case)

Why Was This Recalled?

Package seam of some units may not remain properly sealed to ensure the contents might not be sterile as labeled.

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

About Kimberly-Clark Corporation

Kimberly-Clark Corporation has 19 total recalls tracked by RecallDetector.

Related Recalls

Data sourced from the FDA (Device). Last updated March 26, 2026. View original report