Kimberly-Clark Corporation: Medical Device Recall in 2012 - (Recall #: Z-2425-2012)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2012.

Data Source: FDA.

Product 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 Classification:

Class III

Date Initiated: December 31, 2010

Date Posted: September 26, 2012

Recall Number: Z-2425-2012

Event ID: 62577

Reason for Recall:

The impacted product was not intended for commercial distribution to end users.

Status: Terminated

Product Quantity: 32 cases

Code Information:

Product Code: 95221-35, Unit Code: 90372

Distribution Pattern:

US (nationwide) including the states of CA, CO, LA, NM, OK, TX and WA.

Voluntary or Mandated:

Voluntary: Firm initiated