FDA Adverse Event Malfunction Summary report: N

TOTALCARE

MDR report key: 2257233 · Received September 15, 2011

Report

Report Number
1824206-2011-04784
Event Type
Malfunction
Date Received
September 15, 2011
Date of Event
August 23, 2011
Report Date
August 24, 2011
Manufacturer
HILL-ROM, INC.
Product Code
FNL
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
FL, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

TECHNICIAN CONFIRMED THAT THE SIDERAIL WAS NOT LOCKING IN THE UP RIGHT POSITION DUE TO AGE OF BED. REPLACED LRT LATCH ASSEMBLY TO RESOLVE THIS ISSUE. LOCATION OF BED - PLANT OPS DEPT.

Description of Event or Problem · 1

FACILITY STAFF ALLEGED THAT THE RIGHT SIDERAIL WAS NOT LOCKING IN THE UP RIGHT POSITION. NO INJURY REPORTED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 TOTALCARE AC-POWERED ADJUSTABLE HOSPITAL BED FNL HILL-ROM, INC. P1900

Patients

Seq Age Sex Outcome Treatment
1