FDA Adverse Event Malfunction Summary report: N

MECHANICAL (MANUAL) WHEELCHAIR

MDR report key: 3984395 · Received August 6, 2014

Report

Report Number
9616091-2014-01429
Event Type
Malfunction
Date Received
August 6, 2014
Report Date
June 24, 2014
Manufacturer
INVAMEX
Product Code
IOR
Product Problem
Yes
Report Source
Manufacturer report
Reporter Occupation
OTHER

Narratives

Description of Event or Problem · 1

THE FRAME BROKE BY THE WELD.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
461496 MECHANICAL (MANUAL) WHEELCHAIR 890.3850 IOR INVAMEX T4

Patients

Seq Age Sex Outcome Treatment
1 Other