FDA Adverse Event Malfunction Summary report: N

TOTALCARE BED

MDR report key: 2050151 · Received April 5, 2011

Report

Report Number
1824206-2011-02018
Event Type
Malfunction
Date Received
April 5, 2011
Date of Event
March 14, 2011
Report Date
March 14, 2011
Manufacturer
HILL-ROM INC.
Product Code
FNL
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
OR, US
Reporter Occupation
UNKNOWN

Narratives

Additional Manufacturer Narrative · 1

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

Description of Event or Problem · 1

TECHNICIAN ALLEGED THAT THE HEAD END HI LOW CYLINDER HAD A SLOW DRIFT DOWN. THERE WAS NO PT IMPACT 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