FDA Adverse Event Malfunction Summary report: N

MECHANICAL (MANUAL) WHEELCHAIR

MDR report key: 3222754 · Received July 12, 2013

Report

Report Number
9616091-2013-01202
Event Type
Malfunction
Date Received
July 12, 2013
Report Date
June 19, 2013
Manufacturer
INVAMEX
Product Code
IOR
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
CA, US
Reporter Occupation
PATIENT

Narratives

Description of Event or Problem · 1

DEALER ADVISED BACKCANES ARE BENT AT PUSH HANDLES.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
322528 MECHANICAL (MANUAL) WHEELCHAIR 890.3850 IOR INVAMEX SOLARA3G

Patients

Seq Age Sex Outcome Treatment
1 Other