FDA Adverse Event Malfunction Summary report: N

ADVANTA BED

MDR report key: 2081597 · Received April 13, 2011

Report

Report Number
1824206-2011-02140
Event Type
Malfunction
Date Received
April 13, 2011
Date of Event
March 21, 2011
Report Date
March 21, 2011
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

THE BIOMED VERIFIED THAT VOLTAGE WAS GOING TO THE POWER SUPPLY BOARD AND VOLTAGE COMING OUT OF THE TRANSFORMER. REPAIRS HAVE NOT BEEN COMPLETED.

Description of Event or Problem · 1

THE ACCOUNTS BIOMED ALLEGED THE BED HAS NO FUNCTIONS AND THE POWER SUPPLY BOARD IS CORRODED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 ADVANTA BED AC-POWERED ADJUSTABLE HOSPITAL BED FNL HILL-ROM, INC. 1600

Patients

Seq Age Sex Outcome Treatment
1