FDA Adverse Event Malfunction Summary report: N

NAIL HANDLE

MDR report key: 730130 · Received June 23, 2005

Report

Report Number
9610622-2005-00033
Event Type
Malfunction
Date Received
June 23, 2005
Date of Event
June 5, 2005
Report Date
June 6, 2005
Manufacturer
STRYKER TRAUMA KIEL
Product Code
MDM
Removal / Correction Number
NA
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
MT, US
Reporter Occupation
OTHER

Narratives

Description of Event or Problem · 1

"TARGET ARM WOULD NOT RELEASE FROM NAIL. TAB BROKE OOF WITH NAIL IN THE PT."

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 NAIL HANDLE INSTRUMENT MDM STRYKER TRAUMA KIEL NA K407058

Patients

Seq Age Sex Outcome Treatment
1 UNKNOWN Other