FDA Adverse Event Malfunction Summary report: N

TOTALCARE

MDR report key: 1964136 · Received December 21, 2010

Report

Report Number
1824206-2010-11834
Event Type
Malfunction
Date Received
December 21, 2010
Date of Event
December 10, 2010
Report Date
December 10, 2010
Manufacturer
HILL-ROM INC.
Product Code
FNL
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
TX, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

TECHNICIAN FOUND THAT THE PT RIGHT INTERMEDIATE SIDERAIL LATCH WAS INOPERATIVE. LATCH WAS DIRTY CAUSING RAIL NOT TO LATCH. THE LATCH WAS CLEANED TO RESOLVE THIS ISSUE.

Description of Event or Problem · 1

FACILITY ALLEGED THAT THE SIDE RAIL WOULD NOT STAY ENGAGED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 TOTALCARE AC POWERED ADJUSTABLE HOSPITAL BED FNL HILL-ROM INC. P1900F100

Patients

Seq Age Sex Outcome Treatment
1