FDA Adverse Event Malfunction Summary report: N

TOTALCARE BED

MDR report key: 2842256 · Received November 8, 2012

Report

Report Number
1824206-2012-07293
Event Type
Malfunction
Date Received
November 8, 2012
Date of Event
October 19, 2012
Report Date
October 19, 2012
Manufacturer
HILL-ROM, INC.
Product Code
FNL
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
CA, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

THE HILL-ROM TECHNICIAN CLEANED AND GREASED THE SIDERAIL LATCH AND PIVOT POINTS TO RESOLVE THE ISSUE.

Description of Event or Problem · 1

INFO RECEIVED INDICATED THE RIGHT FOOT SIDERAIL DOES NOT LATCH.

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