FDA Adverse Event Malfunction Summary report: N

TOTALCARE

MDR report key: 1984071 · Received January 14, 2011

Report

Report Number
1824206-2011-00185
Event Type
Malfunction
Date Received
January 14, 2011
Date of Event
December 21, 2010
Report Date
December 21, 2010
Manufacturer
HILL-ROM INC.
Product Code
FNL
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
OR, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

THE TECHNICIAN REPLACED THE HEAD END UP HI/LOW SOLENOID VALVE TO RESOLVE THE ISSUE.

Description of Event or Problem · 1

TECHNICIAN ALLEGED THAT THE HEAD END OF THE BED WOULD NOT RISE. THERE WAS NO PT IMPACT REPORTED.

Devices

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

Patients

Seq Age Sex Outcome Treatment
1