FDA Adverse Event Malfunction Summary report: N

TOTALCARE BED

MDR report key: 2823755 · Received October 10, 2012

Report

Report Number
1824206-2012-06350
Event Type
Malfunction
Date Received
October 10, 2012
Date of Event
September 21, 2012
Report Date
September 21, 2012
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 HILL-ROM TECHNICIAN REPLACED BATTERY TO RESOLVE THE ISSUE.

Description of Event or Problem · 1

INFORMATION RECEIVED INDICATED THAT WHILE THE BED WAS ON BATTERY POWER (MANUAL CONTROL) THE BATTERY LIGHT WAS ON, HOWEVER THE MANUAL FUNCTIONS WOULD NOT OPERATE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 TOTALCARE BED AC-POWERED ADJUSTABLE HOSPITAL BED FNL HILL-ROM INC. 1900

Patients

Seq Age Sex Outcome Treatment
1