FDA Adverse Event Malfunction Summary report: N

POWERED WHEELCHAIR

MDR report key: 3942246 · Received July 17, 2014

Report

Report Number
3008262382-2014-00319
Event Type
Malfunction
Date Received
July 17, 2014
Report Date
June 11, 2014
Manufacturer
INVACARE REHABILITATION EQUIP
Product Code
ITI
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
WA, US
Reporter Occupation
MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

Narratives

Description of Event or Problem · 1

PER TECH DEALER CALLED IN AND STATED THAT THE LEFT MOTOR WILL NOT MOVE WHEN BRAKE IS DISENGAGED. PER TECH DEALER ENDED CALL BEFORE ANY ADDITIONAL INFORMATION COULD BE OBTAINED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
419938 POWERED WHEELCHAIR 890.3860 ITI INVACARE REHABILITATION EQUIP M41SR20R

Patients

Seq Age Sex Outcome Treatment
1 Other