FDA Adverse Event Summary report: N

DAILY ACTIVITY ASSIST DEVICES

MDR report key: 3734071 · Received April 8, 2014

Report

Report Number
1531186-2014-01223
Date Received
April 8, 2014
Report Date
March 10, 2014
Manufacturer
PINGHU WEIFENG MATERIAL TECHNOLOGY
Product Code
IKX
Product Problem
Yes
Report Source
Manufacturer report
Reporter Occupation
MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

Narratives

Description of Event or Problem · 1

IT WAS REPORTED THAT THE SEAT ON A SHOWER CHAIR WAS CRACKED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
212073 DAILY ACTIVITY ASSIST DEVICES 890.5050 IKX PINGHU WEIFENG MATERIAL TECHNOLOGY 96-2

Patients

Seq Age Sex Outcome Treatment
1 Other