FDA Adverse Event Summary report: N

DAILY ACTIVITY ASSIST DEVICES

MDR report key: 4211601 · Received October 29, 2014

Report

Report Number
1531186-2014-05196
Date Received
October 29, 2014
Report Date
October 8, 2014
Manufacturer
UNKNOWN
Product Code
IKX
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
CA
Reporter Occupation
MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

Narratives

Description of Event or Problem · 1

DEALER STATED THAT THE SEAT ON A 96-2 SHOWER CHAIR CRACKED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
692066 DAILY ACTIVITY ASSIST DEVICES 890.5050 IKX UNKNOWN 96-2

Patients

Seq Age Sex Outcome Treatment
1 Other