FDA Adverse Event Summary report: N

DAILY ACTIVITY ASSIST DEVICES

MDR report key: 3811953 · Received May 15, 2014

Report

Report Number
1531186-2014-01792
Date Received
May 15, 2014
Date of Event
March 31, 2014
Report Date
April 7, 2014
Manufacturer
POPULAR PLASTICS
Product Code
IKX
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
MO, US
Reporter Occupation
MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

Narratives

Description of Event or Problem · 1

A 9780 SHOWER CHAIR BROKE UNDER THE SEAT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
290104 DAILY ACTIVITY ASSIST DEVICES 890.5050 IKX POPULAR PLASTICS 9780

Patients

Seq Age Sex Outcome Treatment
1 Other