FDA Adverse Event Malfunction Summary report: N

MECHANICAL (MANUAL) WHEELCHAIR

MDR report key: 3100654 · Received May 8, 2013

Report

Report Number
1525712-2013-03622
Event Type
Malfunction
Date Received
May 8, 2013
Report Date
April 11, 2013
Manufacturer
UNKNOWN
Product Code
IOR
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
CA
Reporter Occupation
MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

Narratives

Description of Event or Problem · 1

PROVIDER STATES SMALL CRACK AT BEND IN CANE, MAKING SQUEAKING NOISE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
200683 MECHANICAL (MANUAL) WHEELCHAIR 890.3850 IOR UNKNOWN UNKNOWN

Patients

Seq Age Sex Outcome Treatment
1 Other