FDA Adverse Event Malfunction Summary report: N

VERSACARE BED

MDR report key: 2024113 · Received March 11, 2011

Report

Report Number
1824206-2011-01498
Event Type
Malfunction
Date Received
March 11, 2011
Date of Event
February 15, 2011
Report Date
February 15, 2011
Manufacturer
HILL-ROM INC.
Product Code
FNL
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
AL, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

REPAIRS HAVE NOT BEEN COMPLETED.

Description of Event or Problem · 1

THE ACCOUNT ALLEGED THE LOCKOUT IS ON, HE GETS 8 FLASH CODE AND NO LIGHTS ARE ON THE POWER SUPPLY. HE LOOKED THE COILED CABLE AND THERE ARE BARE WIRES SHOWING.

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