FDA Adverse Event Malfunction Summary report: N

CENTRA BED

MDR report key: 2933366 · Received December 21, 2012

Report

Report Number
1824206-2012-08453
Event Type
Malfunction
Date Received
December 21, 2012
Date of Event
November 27, 2012
Report Date
November 27, 2012
Manufacturer
HILL-ROM, INC.
Product Code
FNL
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
HI, US
Reporter Occupation
UNKNOWN

Narratives

Additional Manufacturer Narrative · 1

THE TECHNICIAN DEGREASED THE CPR MECHANISM TO REPAIR THE BED.

Description of Event or Problem · 1

INFORMATION RECEIVED INDICATES THE CPR IS SLOW TO LOWER AND IT IS GETTING STUCK.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 CENTRA BED AC-POWERED ADJUSTABLE HOSPITAL BED FNL HILL-ROM, INC. 850

Patients

Seq Age Sex Outcome Treatment
1