FDAApril 2, 2018device
Retractor f/Sciatic Nerve; Part number: 03.100.013; UDI: 10886982070623
Official recall recorded by the U.S. Food & Drug Administration.
The hazard
There is a potential for microspores to form on the hollow handle of the Sciatic Nerve Retractor. The pores may increase in size, allowing fluid to enter the hollow handle.
What to do
FDA enforcement status: Terminated
Brands named
synthes usa productssynthessynthes usa
UPCs
10886982070623
Recall history
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