FDA Adverse Event Malfunction Summary report: N

DAILY ACTIVITY ASSIST DEVICES

MDR report key: 3823918 · Received May 21, 2014

Report

Report Number
9616091-2014-00905
Event Type
Malfunction
Date Received
May 21, 2014
Report Date
April 4, 2014
Manufacturer
INVAMEX
Product Code
ILS
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
IL, US
Reporter Occupation
MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

Narratives

Description of Event or Problem · 1

TBM STATED THAT THE SEAT ON A 9630-4 COMMODE IS BROKEN IN THE MIDDLE WHERE IT MEETS THE LID.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
303185 DAILY ACTIVITY ASSIST DEVICES 890.5050 ILS INVAMEX 9630-4

Patients

Seq Age Sex Outcome Treatment
1 Other