FDA Adverse Event Malfunction Summary report: N

TOTALCARE BED

MDR report key: 2821982 · Received October 1, 2012

Report

Report Number
1824206-2012-06019
Event Type
Malfunction
Date Received
October 1, 2012
Date of Event
September 12, 2012
Report Date
September 12, 2012
Manufacturer
HILL-ROM, INC.
Product Code
FNL
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
GA, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

THE HILL-ROM TECHNICIAN FOUND FLUID ON THE LATCH ASSEMBLY. HE CLEANED AND LUBRICATED THE LATCH ASSEMBLY TO RESOLVE THE ISSUE.

Description of Event or Problem · 1

INFO RECEIVED INDICATED THE RIGHT HEAD SIDERAIL WAS NOT LATCHING.

Devices

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

Patients

Seq Age Sex Outcome Treatment
1