FDA Adverse Event Malfunction Summary report: N

IMMERSION HYDROBATH

MDR report key: 3846039 · Received June 3, 2014

Report

Report Number
1219590-2014-00088
Event Type
Malfunction
Date Received
June 3, 2014
Report Date
April 18, 2014
Manufacturer
INVACARE CLEVELAND STREET
Product Code
ILJ
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
MN, US
Reporter Occupation
MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

Narratives

Description of Event or Problem · 1

CUSTOMER STATES THE DOOR SEAL IS LEAKING.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
324395 IMMERSION HYDROBATH 890.5100 ILJ INVACARE CLEVELAND STREET IH3652G

Patients

Seq Age Sex Outcome Treatment
1 Other