FDAFebruary 22, 2012device
Timberline Cranial Caudal and Posterior Blades, 40 - 180mm Model # 8734-2XXX, 8734-5XXX is a reusable device provided within an aluminum sterilization tray along with other instruments for use in a Timberline procedure Timberline Anchored Lateral Retractable Drills are used with the Timberline La...
Official recall recorded by the U.S. Food & Drug Administration.
The hazard
Biomet Spine, LLC is recalling the Timberline Cranial Caudal and Posterior Blades, 40-180mm due to oversize of the set screw hex feature.
What to do
FDA enforcement status: Terminated
Brands named
biomet spinebiomet
Recall history
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