FDA Adverse Event Malfunction Summary report: N

VERSACARE BED

MDR report key: 2910571 · Received December 3, 2012

Report

Report Number
1824206-2012-07865
Event Type
Malfunction
Date Received
December 3, 2012
Date of Event
November 13, 2012
Report Date
November 13, 2012
Manufacturer
HILL-ROM INC
Product Code
FNL
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
TX, US
Reporter Occupation
UNKNOWN

Narratives

Additional Manufacturer Narrative · 1

THE TECHNICIAN REPLACED THE COMMUNICATION CABLE TO RESOLVE THE ISSUE.

Description of Event or Problem · 1

THE TECHNICIAN ALLEGED THAT THE NURSE CALL SIGNAL IS NOT BEING SENT TO THE NURSE STATION. NO PATIENT IMPACT.

Devices

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

Patients

Seq Age Sex Outcome Treatment
1