FDA Adverse Event Malfunction Summary report: N

POWERED WHEELCHAIR

MDR report key: 3972643 · Received August 1, 2014

Report

Report Number
3008262382-2014-00462
Event Type
Malfunction
Date Received
August 1, 2014
Date of Event
June 18, 2014
Report Date
June 30, 2014
Manufacturer
INVACARE REHABILITATION EQUIP
Product Code
ITI
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
IL, US
Reporter Occupation
PATIENT FAMILY MEMBER OR FRIEND

Narratives

Description of Event or Problem · 1

END USER'S MOTHER STATES THAT CHAIR WILL MOVE A FEW FEET THEN STOP.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
450295 POWERED WHEELCHAIR 890.3860 ITI INVACARE REHABILITATION EQUIP M41SR20B

Patients

Seq Age Sex Outcome Treatment
1 20 Other