FDA Adverse Event Summary report: N

DAILY ACTIVITY ASSIST DEVICES

MDR report key: 3811931 · Received May 15, 2014

Report

Report Number
1531186-2014-01791
Date Received
May 15, 2014
Report Date
April 7, 2014
Manufacturer
UNKNOWN
Product Code
IKX
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
MI, US
Reporter Occupation
MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

Narratives

Description of Event or Problem · 1

DEALER STATED THAT THE SEAT ON A 98071 TRANSFER BENCH IS SPLITTING AT THE SEAM.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
290109 DAILY ACTIVITY ASSIST DEVICES 890.5050 IKX UNKNOWN 98071

Patients

Seq Age Sex Outcome Treatment
1 Other