FDA Adverse Event Summary report: N

DAILY ACTIVITY ASSIST DEVICES

MDR report key: 3787496 · Received May 2, 2014

Report

Report Number
1531186-2014-01609
Date Received
May 2, 2014
Report Date
March 25, 2014
Manufacturer
UNKNOWN
Product Code
IKX
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
OH, US
Reporter Occupation
MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

Narratives

Description of Event or Problem · 1

DEALER STATED THAT A RIVET HOLDING THE LEGS ONTO A (B)(4) SHOWER CHAIR AS BROKEN.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
265700 DAILY ACTIVITY ASSIST DEVICES 890.5050 IKX UNKNOWN 96-2

Patients

Seq Age Sex Outcome Treatment
1 90 Other