FDA Adverse Event Malfunction Summary report: N

MECHANICAL (MANUAL) WHEELCHAIR

MDR report key: 3377160 · Received September 30, 2013

Report

Report Number
1525712-2013-08193
Event Type
Malfunction
Date Received
September 30, 2013
Report Date
September 20, 2013
Manufacturer
INVACARE TAYLOR STREET
Product Code
IOR
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
CA, US
Reporter Occupation
MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

Narratives

Description of Event or Problem · 1

IT WAS REPORTED THAT A MANUAL WHEELCHAIR HAD A BENT FRAME, ARMREST TUBING, FORK, AND SPOKES. ALSO, THE FOLDING BACK OF THE CHAIR WAS NOT STAYING UP; THE CASTERS WERE DAMAGED AND THE WHEELLOCK WAS NOT HOLDING.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
493025 MECHANICAL (MANUAL) WHEELCHAIR 890.3850 IOR INVACARE TAYLOR STREET TA4

Patients

Seq Age Sex Outcome Treatment
1 Other