FDA Adverse Event Malfunction Summary report: N

CENTRA BED

MDR report key: 3003545 · Received February 11, 2013

Report

Report Number
1824206-2013-00949
Event Type
Malfunction
Date Received
February 11, 2013
Date of Event
January 29, 2013
Report Date
January 29, 2013
Manufacturer
HILL-ROM, INC.
Product Code
FNL
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
CO, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

THE TECHNICIAN REPLACED THE POWER CORD PLUG TO RESOLVE THE ISSUE.

Description of Event or Problem · 1

THE TECH ALLEGED THE BED HAS A LOSS OF GROUND. NO PATIENT IMPACT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
59206 CENTRA BED A/C POWERED ADJUSTABLE HOSPITAL BED FNL HILL-ROM, INC. 850

Patients

Seq Age Sex Outcome Treatment
1