FDA Adverse Event Malfunction Summary report: N

SAWBLADE NEW Z STYLE 25WX050

MDR report key: 950475 · Received September 1, 2004

Report

Report Number
2249697-2004-00109
Event Type
Malfunction
Date Received
September 1, 2004
Date of Event
August 4, 2004
Report Date
August 4, 2004
Manufacturer
STRYKER ORTHOPAEDICS
Product Code
DZH
Removal / Correction Number
NA
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
VA, US
Reporter Occupation
OTHER

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 SAWBLADE NEW Z STYLE 25WX050 INSTRUMENT DZH STRYKER ORTHOPAEDICS NA 033463LO

Patients

Seq Age Sex Outcome Treatment
1 NO INFO Other