FDA Adverse Event Malfunction Summary report: N

MECHANICAL (MANUAL) WHEELCHAIR

MDR report key: 3112824 · Received May 14, 2013

Report

Report Number
9616091-2013-00825
Event Type
Malfunction
Date Received
May 14, 2013
Report Date
April 18, 2013
Manufacturer
INVAMEX
Product Code
IOR
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
KY, US
Reporter Occupation
OTHER

Narratives

Description of Event or Problem · 1

PER FACILITY A MAN SAID HE BRUISED HIS HAND WHILE TRYING TO PUSH DOWN THE WHEEL LOCK. SHE DID NOT HAVE THE PATIENT'S NAME AND THE FACILITY DID NOT WANT TO COMPLETE FORM.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
212776 MECHANICAL (MANUAL) WHEELCHAIR 890.3850 IOR INVAMEX TRSX5

Patients

Seq Age Sex Outcome Treatment
1 Other