FDA Adverse Event Malfunction Summary report: N

IMMERSION HYDROBATH

MDR report key: 3981114 · Received August 5, 2014

Report

Report Number
1219590-2014-00114
Event Type
Malfunction
Date Received
August 5, 2014
Report Date
June 27, 2014
Manufacturer
INVACARE CLEVELAND STREET
Product Code
ILJ
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
WI, US
Reporter Occupation
MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

Narratives

Description of Event or Problem · 1

IT WAS REPORTED THAT THE IH3650 TUB DOOR SEAL IS LEAKING.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
457005 IMMERSION HYDROBATH 890.5100 ILJ INVACARE CLEVELAND STREET IH3650

Patients

Seq Age Sex Outcome Treatment
1 Other