inforMED
MalfunctionHTY

KIRSCHNER WIRES

Received Oct 23, 2017 · Event occurred Feb 17, 2017

Report 6968200 · MDR key 6968200

Device

Generic name

Wire, Surgical

Manufacturer

Zimmer, Inc.

Product problems

  • Break
  • Difficult to Remove

Patient

Not reported

  • Device Embedded In Tissue or Plaque
  • Device Embedded In Tissue or Plaque

Narrative

Description of Event or Problem

PATIENT UNDERWENT A POSTERIOR SPINAL FUSION WITH SEGMENTAL INSTRUMENTATION. A GUIDE WIRE DESIGNED TO HELP THREAD THE PEDICLE SCREW BROKE AND WAS RETAINED. SURGEON'S DECISION WAS TO LEAVE THE GUIDE WIRE IN PLACE AS THERE WAS NO HARM TO THE PATIENT.