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Kimberly-Clark Corporation recalls ULTRA Fabric Reinforced surgical Gown X-Large Sterile The product is a sterile, single use, surgical gown intended to
Recalled November 14, 2012 · FDA recall Z-0257-2013 · Kimberly-Clark
Hazard
Package seam of some units may not remain properly sealed to ensure the contents might not be sterile as labeled. · FDA Class II
Units
89,856 (28 units per case)
Sold at
Nationwide Distribution
Description
Package seam of some units may not remain properly sealed to ensure the contents might not be sterile as labeled.
Product
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.
Manufacturer(s)
Kimberly-Clark Corporation
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →