FDA Adverse Event Malfunction Summary report: N

MECHANICAL (MANUAL) WHEELCHAIR

MDR report key: 3024304 · Received March 27, 2013

Report

Report Number
9616091-2013-00525
Event Type
Malfunction
Date Received
March 27, 2013
Report Date
March 1, 2013
Manufacturer
INVAMEX
Product Code
IOR
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
IA, US
Reporter Occupation
MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

Narratives

Description of Event or Problem · 1

(B)(4). NO SERIOUS INJURY ALLEGED. MALFUNCTION ALLEGED. PER PROVIDER THE RECEPTACLE WHICH SECURES THE BACK CANES TO THE SIDE FRAME BROKE OFF. MDR FILED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
125898 MECHANICAL (MANUAL) WHEELCHAIR 890.3850 IOR INVAMEX 9XT

Patients

Seq Age Sex Outcome Treatment
1 Other