FDA Adverse Event Malfunction Summary report: N

MECHANICAL (MANUAL) WHEELCHAIR

MDR report key: 3833322 · Received May 27, 2014

Report

Report Number
9616091-2014-00940
Event Type
Malfunction
Date Received
May 27, 2014
Date of Event
March 3, 2014
Report Date
March 3, 2014
Manufacturer
INVAMEX
Product Code
IOR
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
SN
Reporter Occupation
MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

Narratives

Description of Event or Problem · 1

DEALER STATED THAT THE FOOTREST ON A (B)(4) WHEELCHAIR WILL NOT LOCK INTO PLACE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
310705 MECHANICAL (MANUAL) WHEELCHAIR 890.3850 IOR INVAMEX 9XDT

Patients

Seq Age Sex Outcome Treatment
1 Other