FDA Adverse Event Summary report: N

DAILY ACTIVITY ASSIST DEVICES

MDR report key: 3241833 · Received July 22, 2013

Report

Report Number
1531186-2013-03289
Date Received
July 22, 2013
Report Date
July 2, 2013
Manufacturer
POPULAR PLASTICS
Product Code
IKX
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
WA, US
Reporter Occupation
MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

Narratives

Description of Event or Problem · 1

IT WAS REPORTED THAT A 9780 SHOWER CHAIR HAD A CRACKED SEAT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
341040 DAILY ACTIVITY ASSIST DEVICES 890.5050 IKX POPULAR PLASTICS 9780

Patients

Seq Age Sex Outcome Treatment
1 Other