FDA Adverse Event Malfunction Summary report: N

TOTALCARE

MDR report key: 2241353 · Received September 2, 2011

Report

Report Number
1824206-2011-04623
Event Type
Malfunction
Date Received
September 2, 2011
Date of Event
August 16, 2011
Report Date
August 16, 2011
Manufacturer
HILL-ROM INC.
Product Code
FNL
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
WA, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

THE TECHNICIAN ISOLATED THE ISSUE TO THE SIDERAIL LATCH STICKING. HE LUBRICATED THE LATCH ASSEMBLY TO REPAIR THE BED.

Description of Event or Problem · 1

INFO RECEIVED INDICATES THE LEFT HEAD SIDERAIL IS NOT LATCHING.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 TOTALCARE AC-POWERED ADJUSTABLE HOSPITAL BED FNL HILL-ROM INC. 1900

Patients

Seq Age Sex Outcome Treatment
1