FDA Adverse Event Malfunction Summary report: N

SITZ BATH 1616700692

MDR report key: 5056816 · Received September 4, 2015

Report

Report Number
1219590-2015-00138
Event Type
Malfunction
Date Received
September 4, 2015
Report Date
August 10, 2015
Manufacturer
INVACARE CLEVELAND STREET
Product Code
KTC
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
WI, US
Reporter Occupation
MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

Narratives

Additional Manufacturer Narrative · 1

SHOULD ADDITIONAL INFORMATION BECOME AVAILABLE A SUPPLEMENTAL RECORD WILL BE FILED.

Description of Event or Problem · 1

TUB HAS A SEAL WHICH IS COMING OFF OF THE TUB DOOR.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
589619 SITZ BATH 1616700692 BATH, SITZ, NONPOWERED KTC INVACARE CLEVELAND STREET IH3652G

Patients

Seq Age Sex Outcome Treatment
1 Other