FDA Adverse Event Malfunction Summary report: N

MECHANICAL (MANUAL) WHEELCHAIR

MDR report key: 3191512 · Received June 26, 2013

Report

Report Number
1525712-2013-05025
Event Type
Malfunction
Date Received
June 26, 2013
Report Date
May 31, 2013
Manufacturer
INVACARE TAYLOR STREET
Product Code
IOR
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
MI, US
Reporter Occupation
MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

Narratives

Description of Event or Problem · 1

PROVIDER STATES THE CONSUMER LEANS ON THE ARMS AND THEY BENT THE ARM TUBE WHICH CAUSED THE SCREWS TO BREAK.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
291543 MECHANICAL (MANUAL) WHEELCHAIR 890.3850 IOR INVACARE TAYLOR STREET SOLARA3G

Patients

Seq Age Sex Outcome Treatment
1 Other