FDA Adverse Event Malfunction Summary report: N

VERSACARE BED

MDR report key: 3112015 · Received May 2, 2013

Report

Report Number
1824206-2013-02445
Event Type
Malfunction
Date Received
May 2, 2013
Date of Event
April 10, 2013
Report Date
April 10, 2013
Manufacturer
HILL-ROM, INC.
Product Code
FNL
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
MD, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

NO FURTHER INFORMATION IS AVAILABLE ON THE REPAIR OF THE BED AT THIS TIME.

Description of Event or Problem · 1

THE ACCOUNT ALLEGED THAT THE BED IS NOT SENDING A NURSE CALL WHEN THE PATIENT POSITION MODULE IS ALARMING. NO INJURY REPORTED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
193435 VERSACARE BED A/C POWERED ADJUSTABLE HOSPITAL BED FNL HILL-ROM, INC. 3200

Patients

Seq Age Sex Outcome Treatment
1