FDA Adverse Event Malfunction Summary report: N

DAILY ACTIVITY ASSIST DEVICES

MDR report key: 3180700 · Received June 20, 2013

Report

Report Number
9616091-2013-01044
Event Type
Malfunction
Date Received
June 20, 2013
Report Date
May 23, 2013
Manufacturer
INVAMEX
Product Code
ILS
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

PROVIDER STATES THE TOILET SEAT IS CRACKED. "TOILET SEAT WITH LID" P/N 1112182.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
280842 DAILY ACTIVITY ASSIST DEVICES 890.5050 ILS INVAMEX UNKNOWN

Patients

Seq Age Sex Outcome Treatment
1 Other