FDA Adverse Event Malfunction Summary report: N

DAILY ACTIVITY ASSIST DEVICES

MDR report key: 3844615 · Received June 3, 2014

Report

Report Number
9616091-2014-00974
Event Type
Malfunction
Date Received
June 3, 2014
Report Date
April 17, 2014
Manufacturer
INVAMEX
Product Code
IKX
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
TN, US
Reporter Occupation
MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

Narratives

Description of Event or Problem · 1

TRANSFER BENCH HAS CRACKED WHERE THE HARDWARE ATTACHES.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
323989 DAILY ACTIVITY ASSIST DEVICES 890.5050 IKX INVAMEX 9670C

Patients

Seq Age Sex Outcome Treatment
1 Other