FDA Adverse Event Malfunction Summary report: N

MECHANICAL (MANUAL) WHEELCHAIR

MDR report key: 4240711 · Received November 10, 2014

Report

Report Number
9616091-2014-02415
Event Type
Malfunction
Date Received
November 10, 2014
Report Date
October 21, 2014
Manufacturer
INVAMEX
Product Code
IOR
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
MA, US
Reporter Occupation
MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

Narratives

Description of Event or Problem · 1

PROVIDER ALLEGES THAT THE LEFT LEGREST ASSEMBLY WILL NOT LOCK INTO PLACE ON THE 9TPZ WHEELCHAIR.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
724175 MECHANICAL (MANUAL) WHEELCHAIR 890.3850 IOR INVAMEX 9TPZ

Patients

Seq Age Sex Outcome Treatment
1 Other