FDA Adverse Event Malfunction Summary report: N

MECHANICAL (MANUAL) WHEELCHAIR

MDR report key: 3033981 · Received April 3, 2013

Report

Report Number
1525712-2013-02549
Event Type
Malfunction
Date Received
April 3, 2013
Report Date
March 7, 2013
Manufacturer
UNKNOWN
Product Code
IOR
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
PA, US
Reporter Occupation
MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

Narratives

Description of Event or Problem · 1

(B)(4). NO SERIOUS INJURY ALLEGED. MALFUNCTION ALLEGED. PROVIDER STATED SOMETHING HAPPENED TO THE CASTER AND IT WOULD NOT TURN. MDR FILED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
137236 MECHANICAL (MANUAL) WHEELCHAIR 890.3850 IOR UNKNOWN UNKNOWN

Patients

Seq Age Sex Outcome Treatment
1 Other