FDA Adverse Event Malfunction Summary report: N

MECHANICAL (MANUAL) WHEELCHAIR

MDR report key: 4203358 · Received October 27, 2014

Report

Report Number
9616091-2014-02268
Event Type
Malfunction
Date Received
October 27, 2014
Report Date
October 7, 2014
Manufacturer
INVAMEX
Product Code
IOR
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
PA, US
Reporter Occupation
MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

Narratives

Description of Event or Problem · 1

PER PROVIDER, OUT OF THE BOX THE RIGHT SIDE OF THE FRAME IS BENT. THEY CAN OPEN THE CHAIR UP, BUT IT VEERS TO THE RIGHT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
683860 MECHANICAL (MANUAL) WHEELCHAIR 890.3850 IOR INVAMEX 9TPZ

Patients

Seq Age Sex Outcome Treatment
1 Other