FDA Adverse Event Malfunction Summary report: N

TOTALCARE

MDR report key: 2010249 · Received March 1, 2011

Report

Report Number
1824206-2011-01175
Event Type
Malfunction
Date Received
March 1, 2011
Date of Event
February 11, 2011
Report Date
February 11, 2011
Manufacturer
HILL-ROM INC.
Product Code
FNL
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
MD, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

TECHNICIAN FOUND ONLY PROBLEM WITH THE BED WAS THAT THE HEAD RIGHT SIDERAIL WOULD NOT GO UP, DUE TO A BENT "METAL DROP PLATE". ADJUSTED DROP PLATE TO WHERE SIDERAIL WAS ABLE TO GO UP OR DOWN FREELY TO RESOLVE THIS ISSUE.

Description of Event or Problem · 1

COMPLAINT ALLEGED THAT THE BED WAS NOT WORKING, NO OTHER INFO GIVEN.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 TOTALCARE AC POWERED ADJUSTABLE HOSPITAL BED FNL HILL-ROM INC. P1840RE200

Patients

Seq Age Sex Outcome Treatment
1