FDA Adverse Event Malfunction Summary report: N

MECHANICAL (MANUAL) WHEELCHAIR

MDR report key: 3961897 · Received July 28, 2014

Report

Report Number
9616091-2014-01324
Event Type
Malfunction
Date Received
July 28, 2014
Report Date
June 20, 2014
Manufacturer
INVAMEX
Product Code
IOR
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
NC, US
Reporter Occupation
MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

Narratives

Description of Event or Problem · 1

DEALER STATES THE LEFT FORK IS BENT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
438070 MECHANICAL (MANUAL) WHEELCHAIR 890.3850 IOR INVAMEX T424HD280

Patients

Seq Age Sex Outcome Treatment
1 Other