FDA Adverse Event Summary report: N

K-WIRE

MDR report key: 1062198 · Received June 10, 2008

Report

Report Number
1062198
Date Received
June 10, 2008
Date of Event
May 29, 2008
Report Date
June 10, 2008
Manufacturer
SMITH & NEPHEW, INC.
Product Code
HTY
Report Source
User Facility report
Reporter Location
RI, US
Reporter Occupation
RISK MANAGER

Narratives

Description of Event or Problem · 1

DURING SURGERY, THE K-WIRE TIP BROKE OFF IN THE PATIENT'S BONE. STAFF WAS UNABLE TO RETRIEVE THE TIP.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 K-WIRE GUIDEWIRE HTY SMITH & NEPHEW, INC. UNK UNK

Patients

Seq Age Sex Outcome Treatment
1 90 YR