FDA Adverse Event Malfunction Summary report: N

IMMERSION HYDROBATH

MDR report key: 3230577 · Received July 16, 2013

Report

Report Number
1219590-2013-00060
Event Type
Malfunction
Date Received
July 16, 2013
Report Date
June 25, 2013
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

DOOR SEAL LEAKS.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
330010 IMMERSION HYDROBATH 890.5100 ILJ INVACARE CLEVELAND STREET IH3652G

Patients

Seq Age Sex Outcome Treatment
1 Other