FDA Adverse Event Malfunction Summary report: N

IMMERSION HYDROBATH

MDR report key: 3936030 · Received July 15, 2014

Report

Report Number
1219590-2014-00103
Event Type
Malfunction
Date Received
July 15, 2014
Report Date
June 10, 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

DEALER ALLEGED THAT THE TUB DOOR IS LEAKING.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
414183 IMMERSION HYDROBATH 890.5100 ILJ INVACARE CLEVELAND STREET IH3652G

Patients

Seq Age Sex Outcome Treatment
1 Other