FDA Adverse Event Malfunction Summary report: N

TOTALCARE BED

MDR report key: 2559771 · Received April 19, 2012

Report

Report Number
1824206-2012-02187
Event Type
Malfunction
Date Received
April 19, 2012
Date of Event
April 2, 2012
Report Date
April 2, 2012
Manufacturer
HILL-ROM, INC.
Product Code
FNL
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
FL, US
Reporter Occupation
UNKNOWN

Narratives

Additional Manufacturer Narrative · 1

THE TECHNICIAN TRIED TO RAISE THE HEAD OF THE BED MANUALLY AND THERE WAS NO CHANGE. THE TECHNICIAN REPLACED THE HEAD UP VALVE CARTRIDGE TO RESOLVE THE ISSUE.

Description of Event or Problem · 1

TECHNICIAN ALLEGED NO HED UP FUNCTION. NO INJURY REPORTED.

Devices

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

Patients

Seq Age Sex Outcome Treatment
1