FDA Adverse Event Malfunction Summary report: N

MECHANICAL (MANUAL) WHEELCHAIR

MDR report key: 3071913 · Received April 22, 2013

Report

Report Number
9616091-2013-00675
Event Type
Malfunction
Date Received
April 22, 2013
Report Date
March 27, 2013
Manufacturer
INVAMEX
Product Code
IOR
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
FL, US
Reporter Occupation
MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

Narratives

Additional Manufacturer Narrative · 1

(B)(4). THE MALFUNCTION HAS NOT BEEN CONFIRMED.

Description of Event or Problem · 1

DEALER STATES THE RIGHT ELEVATING LEGREST IS NOT WORKING AND WANTS ANOTHER ONE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
171132 MECHANICAL (MANUAL) WHEELCHAIR 890.3850 IOR INVAMEX SOLARA3G

Patients

Seq Age Sex Outcome Treatment
1 Other