FDA Adverse Event Malfunction Summary report: N

MECHANICAL (MANUAL) WHEELCHAIR

MDR report key: 3971053 · Received July 31, 2014

Report

Report Number
9616091-2014-01363
Event Type
Malfunction
Date Received
July 31, 2014
Date of Event
June 20, 2014
Report Date
June 20, 2014
Manufacturer
INVAMEX
Product Code
IOR
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
MO, US
Reporter Occupation
MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

Narratives

Description of Event or Problem · 1

DEALER ALLEGED THAT THE TRANS WHEEL LOCK WILL NOT STAY IN PLACE AND THE HANDLE KEEPS SLIPPING OUT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
448331 MECHANICAL (MANUAL) WHEELCHAIR 890.3850 IOR INVAMEX 9XT

Patients

Seq Age Sex Outcome Treatment
1 Other