FDA Adverse Event Malfunction Summary report: N

MECHANICAL (MANUAL) WHEELCHAIR

MDR report key: 2895690 · Received January 3, 2013

Report

Report Number
1525712-2013-00048
Event Type
Malfunction
Date Received
January 3, 2013
Report Date
January 3, 2013
Manufacturer
INVACARE TAYLOR STREET
Product Code
IOR
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
KY, US
Reporter Occupation
MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

Narratives

Description of Event or Problem · 1

ALUMINUM HANDRIM BROKE WHERE THE RIM CIRCLE GETS WELDED TOGETHER TO COMPLETE THE CIRCLE. ALSO THE FOOTRESTS ARE BENT. NO INJURY. THIS DEVICE IS USED IN A FACILITY FOR CLIENTS WITH BRAIN INJURY.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
2417 MECHANICAL (MANUAL) WHEELCHAIR 890.3850 IOR INVACARE TAYLOR STREET MVPS

Patients

Seq Age Sex Outcome Treatment
1 Other