FDA Adverse Event Malfunction Summary report: N

VERSACARE BED

MDR report key: 2130343 · Received May 9, 2011

Report

Report Number
1824206-2011-02624
Event Type
Malfunction
Date Received
May 9, 2011
Date of Event
April 15, 2011
Report Date
April 15, 2011
Manufacturer
HILL-ROM, INC.
Product Code
FNL
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
SD, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

REPAIRS HAVE NOT BEEN COMPLETED.

Description of Event or Problem · 1

THE ACCOUNT'S MAINTENANCE STATED WHEN HE LOWERED THE RIGHT HEAD SIDERAIL, THE HEAD RAN UP UNINTENTIONALLY. HE HAS REPLACED THE RIGHT SIDERAIL CABLE BUT NOT THE SVC REQUIRED IS FLASHING AN ERROR CODE OF 4 (RIGHT CAREGIVER NODE).

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