FDA Adverse Event Summary report: N

DAILY ACTIVITY ASSIST DEVICES

MDR report key: 3130484 · Received May 24, 2013

Report

Report Number
1531186-2013-02317
Date Received
May 24, 2013
Report Date
May 1, 2013
Manufacturer
SHUNLONG PHYSICAL THERAPY EQUIPMENT
Product Code
IKX
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
PA, US
Reporter Occupation
MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

Narratives

Description of Event or Problem · 1

DEALER STATES SEAT CRACKED ON A 6358 SHOWER COMMODE CHAIR.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
231566 DAILY ACTIVITY ASSIST DEVICES 890.5050 IKX SHUNLONG PHYSICAL THERAPY EQUIPMENT 6358

Patients

Seq Age Sex Outcome Treatment
1 Other