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Smith & Nephew, Inc. Endoscopy Division recalls SUTUREFIX Ultra Anchor XL with one (#2) Ultrabraid Cobraid Suture Product Code: 72203842 Fastener, fixation, nondegr
Recalled July 23, 2014 · FDA recall Z-2046-2014 · Smith & Nephew, Inc. Endoscopy Division
Hazard
Sterility of device is compromised due to breach in sterile barrier · FDA Class II
Units
136 units
Sold at
Worldwide Distribution - USA (nationwide) and Internationally to Australia, Belgium, Denmark, France, Germany, Great Britain, Italy, Netherlands, Norway, Portugal, Spain, and Sweden.
Description
Sterility of device is compromised due to breach in sterile barrier
Product
SUTUREFIX Ultra Anchor XL with one (#2) Ultrabraid Cobraid Suture Product Code: 72203842 Fastener, fixation, nondegradable, soft tissue
Manufacturer(s)
Smith & Nephew, Inc. Endoscopy Division
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →