FDA Adverse Event Malfunction Summary report: N

HLL-ROM 100 LOW BED

MDR report key: 1794987 · Received August 9, 2010

Report

Report Number
1824206-2010-09214
Event Type
Malfunction
Date Received
August 9, 2010
Date of Event
July 12, 2010
Report Date
July 12, 2010
Manufacturer
HILL-ROM, INC.
Product Code
FNL
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
LA, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

THE TECHNICIAN REPLACED THE MAIN CONTROLLER TO REPAIR THE BED.

Description of Event or Problem · 1

INFORMATION RECEIVED INDICATES THE BED HAS NO FUNCTIONS.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 HLL-ROM 100 LOW BED AC POWERED HOSPITAL BED FNL HILL-ROM, INC. 3930

Patients

Seq Age Sex Outcome Treatment
1 UNK