FDA Adverse Event Summary report: N

CANES

MDR report key: 3033972 · Received April 3, 2013

Report

Report Number
1531186-2013-01395
Date Received
April 3, 2013
Report Date
March 7, 2013
Manufacturer
UNKNOWN
Product Code
IPS
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
OH, US
Reporter Occupation
PATIENT

Narratives

Description of Event or Problem · 1

PER CONSUMER CAM LOCK BROKE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
137230 CANES 890.3075 IPS UNKNOWN 40918-6

Patients

Seq Age Sex Outcome Treatment
1 76 Other