FDA Adverse Event Malfunction Summary report: N

VERSACARE BED

MDR report key: 2112431 · Received April 28, 2011

Report

Report Number
1824206-2011-02431
Event Type
Malfunction
Date Received
April 28, 2011
Date of Event
April 4, 2011
Report Date
April 4, 2011
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 TECHNICIAN FOUND THE GROUND PIN ON THE POWER CORD WAS LOOSE. THE TECHNICIAN REPLACED THE POWER CORD TO REPAIR THE BED.

Description of Event or Problem · 1

INFORMATION RECEIVED INDICATES THE BED HAS NO GROUND.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 VERSACARE BED AC-POWERED ADJUSTABLE HOSPITAL BED FNL HILL-ROM, INC. 3200

Patients

Seq Age Sex Outcome Treatment
1