FDA Adverse Event Malfunction Summary report: N

TOTALCARE

MDR report key: 2063130 · Received March 16, 2011

Report

Report Number
1824206-2011-01613
Event Type
Malfunction
Date Received
March 16, 2011
Date of Event
February 25, 2011
Report Date
February 25, 2011
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

TECHNICIAN FOUND THAT THE HEAD OF THE BED WAS NOT GOING UP, NO MANUAL FUNCTIONS. REPLACED THE MANIFOLD TO RESOLVE THIS ISSUE. BED WAS LOCATED IN ICU.

Description of Event or Problem · 1

COMPLAINT ALLEGED THAT THE HEAD OF BED WAS NOT GOING UP.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 TOTALCARE AC POWERED ADJUSTABLE HOSPITAL BED FNL HILL-ROM, INC. P1900

Patients

Seq Age Sex Outcome Treatment
1