FDA Adverse Event Malfunction Summary report: N

ZIMMER NATURAL NAIL CEPHALOMEDULLARY GUIDE

MDR report key: 3162138 · Received June 6, 2013

Report

Report Number
1822565-2013-00938
Event Type
Malfunction
Date Received
June 6, 2013
Date of Event
May 6, 2013
Report Date
May 8, 2013
Manufacturer
ZIMMER, INC.
Product Code
HSB
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
KS, US
Reporter Occupation
PHYSICIAN

Narratives

Additional Manufacturer Narrative · 1

THIS REPORT WILL BE AMENDED WHEN OUR INVESTIGATION IS COMPLETE.

Description of Event or Problem · 1

IT IS REPORTED THAT THE SURGEON STRUGGLED TO GET THE NAIL THROUGH THE TARGETING GUIDE HOLE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
250619 ZIMMER NATURAL NAIL CEPHALOMEDULLARY GUIDE HSB ZIMMER, INC. 61613525

Patients

Seq Age Sex Outcome Treatment
1 47 YR