FDA Adverse Event Malfunction Summary report: N

ADVANTA BED

MDR report key: 1900838 · Received November 9, 2010

Report

Report Number
1824206-2010-10939
Event Type
Malfunction
Date Received
November 9, 2010
Date of Event
October 14, 2010
Report Date
October 14, 2010
Manufacturer
HILL-ROM, INC.
Product Code
FNL
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
CA, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

THE TECH ISOLATED THE UNINTENTIONAL MOVEMENT TO THE CPR LIMIT SWITCH. HE REPLACED THE CPR SWITCH TO REPAIR THIS BED.

Description of Event or Problem · 1

INFO RECEIVED INDICATES THE HEAD SECTION HAD AN UNINTENTIONAL MOVEMENT OF THE HEAD DOWN FUNCTION. THE HEAD SECTION WOULD RISE APPROX TO 30 DEGREES AND THEN RUN BACK TO THE LOWEST POSITION.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 ADVANTA BED AC-POWERED ADJUSTABLE HOSPITAL BED FNL HILL-ROM, INC. 1604

Patients

Seq Age Sex Outcome Treatment
1