inforMED
MalfunctionHXY

CASPAR

Received Mar 16, 2011 · Event occurred Feb 23, 2011

Report 2024467 · MDR key 2024467

Device

Generic name

Drill Guide

Manufacturer

Aesculap

Model number

FF 907

Catalog number

FF 907

Lot number

AN HOD

Product problems

  • Break

Patient

62 YR

  • No Known Impact Or Consequence To Patient

Narrative

Description of Event or Problem

FEMALE PATIENT SCHEDULED FOR FUSION OF CERVICAL VERTEBRA C5-C6, C6-C7 (ANTERIOR MULTI LEVEL). DRILL GUIDE FROM THE ANTERIOR CERVICAL SET BROKE INTRAOPERATIVELY. PIECES OF THE DRILL GUIDE WERE RECOVERED.