FDA Adverse Event Malfunction Summary report: N

XIA II PA SCREWDRIVER SHAFT

MDR report key: 1000540 · Received February 15, 2008

Report

Report Number
9617544-2008-00014
Event Type
Malfunction
Date Received
February 15, 2008
Date of Event
November 6, 2007
Report Date
January 27, 2008
Manufacturer
STRYKER SPINE BORDEAUX
Product Code
HXX
Removal / Correction Number
NA
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
KS
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

NA

Description of Event or Problem · 1

DURING SURGERY, THE TIP OF THE SCREWDRIVER BROKE. A PIECE OF THE BROKEN PART FELL INTO THE PT'S BODY AND THE SURGEON REMOVED IT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 XIA II PA SCREWDRIVER SHAFT INSTRUMENT HXX STRYKER SPINE BORDEAUX NA 040753

Patients

Seq Age Sex Outcome Treatment
1 UNK Other