Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-0258-2013 — MicroCool Breathable Gown with Towels, X-Larg, X-Long, 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.

U.S. FDA — Device Enforcement · United States · 2012-07-05 · Class II

AI-assisted, human-edited — this page is drafted with AI from public-source data, then reviewed before publication. How we use AI →
Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0258-2013
Date of alert
2012-07-05
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Kimberly-Clark Corporation
Product category
device
Product type
Devices
Reported risk: Package seam of some units may not remain properly sealed to ensure the contents might not be sterile as labeled.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.