FDA Adverse Event Summary report: N

CANES

MDR report key: 3103291 · Received May 9, 2013

Report

Report Number
1531186-2013-01975
Date Received
May 9, 2013
Report Date
April 15, 2013
Manufacturer
UNKNOWN
Product Code
IPS
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
GA, US
Reporter Occupation
PATIENT

Narratives

Description of Event or Problem · 1

PER END USER WELD IS BROKEN.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
203476 CANES 890.3075 IPS UNKNOWN 7827

Patients

Seq Age Sex Outcome Treatment
1 85 Other