FDA Adverse Event Malfunction Summary report: N

POWERED WHEELCHAIR

MDR report key: 2874261 · Received December 14, 2012

Report

Report Number
1525712-2012-02979
Event Type
Malfunction
Date Received
December 14, 2012
Report Date
December 14, 2012
Manufacturer
INVACARE TAYLOR STREET
Product Code
ITI
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
NJ, US
Reporter Occupation
MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

Narratives

Additional Manufacturer Narrative · 1

(B)(4) KEL - NO RMA HAS BEEN INITIATED FOR THIS ISSUE. THE CONSUMER'S AGE, HEIGHT AND WEIGHT ARE UNKNOWN. THE CONSUMER'S MEDICAL CONDITION, STABILITY AND MEDICATION REGIMEN ARE UNKNOWN. THE CONSUMER'S TECHNIQUE WHILE USING THE DEVICE IS UNKNOWN. THE MAINTENANCE HISTORY OF THE DEVICE IS UNKNOWN. THE MALFUNCTION HAS NOT BEEN CONFIRMED.

Description of Event or Problem · 1

DEALER STATED THAT THE WHEEL TUBE ON A M91PR POWER CHAIR WENT FLAT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 POWERED WHEELCHAIR 890.3860 ITI INVACARE TAYLOR STREET M91R

Patients

Seq Age Sex Outcome Treatment
1 Other