FDA Adverse Event Malfunction Summary report: N

VERSACARE BED

MDR report key: 2002974 · Received February 8, 2011

Report

Report Number
1824206-2011-00726
Event Type
Malfunction
Date Received
February 8, 2011
Date of Event
January 13, 2011
Report Date
January 13, 2011
Manufacturer
HILL-ROM INC.
Product Code
FNL
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
SC, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

THE ACCOUNT INSTALLED THE MISSING SCREW LOCKS TO REPAIR THE BED.

Description of Event or Problem · 1

THE ACCOUNT ALLEGED THAT THE COMMUNICATION CABLE WASN'T STAYING CONNECTED TO THE BED DUE TO ONE OF THE SCREWS MISSING FROM THE CABLE ASSEMBLY. THE CABLE COMING LOOSE WOULD NOT ALLOW A NURSE CALL SIGNAL TO BE SENT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 VERSACARE BED MED SURGICAL FNL HILL-ROM INC. 3200

Patients

Seq Age Sex Outcome Treatment
1