FDA Adverse Event Malfunction Summary report: N

IMMERSION HYDROBATH

MDR report key: 4221196 · Received November 3, 2014

Report

Report Number
1219590-2014-00184
Event Type
Malfunction
Date Received
November 3, 2014
Report Date
October 15, 2014
Manufacturer
INVACARE CLEVELAND STREET
Product Code
ILJ
Product Problem
Yes
Report Source
Manufacturer report
Reporter Occupation
MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

Narratives

Description of Event or Problem · 1

PER PROVIDER, DOOR SEAL LEAKING.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
703356 IMMERSION HYDROBATH 890.5100 ILJ INVACARE CLEVELAND STREET IH3652G

Patients

Seq Age Sex Outcome Treatment
1 Other