FDA Adverse Event Malfunction Summary report: N

MECHANICAL (MANUAL) WHEELCHAIR

MDR report key: 3931135 · Received July 14, 2014

Report

Report Number
1525712-2014-03631
Event Type
Malfunction
Date Received
July 14, 2014
Report Date
June 6, 2014
Manufacturer
UNKNOWN
Product Code
IOR
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
NY, US
Reporter Occupation
OTHER

Narratives

Description of Event or Problem · 1

PROVIDER STATES THE WHEEL IS BROKEN.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
410578 MECHANICAL (MANUAL) WHEELCHAIR 890.3850 IOR UNKNOWN UNKNOWN

Patients

Seq Age Sex Outcome Treatment
1 Other