FDA Adverse Event Malfunction Summary report: N

POWERED WHEELCHAIR

MDR report key: 3051772 · Received April 10, 2013

Report

Report Number
1525712-2013-02761
Event Type
Malfunction
Date Received
April 10, 2013
Report Date
March 14, 2013
Manufacturer
UNKNOWN
Product Code
ITI
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

(B)(4). NO SERIOUS INJURY ALLEGED. MALFUNCTION ALLEGED. PROVIDER STATES CHAIR PULLING TO THE RIGHT. MDR FILED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
149024 POWERED WHEELCHAIR 890.3860 ITI UNKNOWN M51

Patients

Seq Age Sex Outcome Treatment
1 Other