FDA Adverse Event Malfunction Summary report: N

TOTALCARE BED

MDR report key: 3033298 · Received March 1, 2013

Report

Report Number
1824206-2013-01163
Event Type
Malfunction
Date Received
March 1, 2013
Date of Event
February 4, 2013
Report Date
February 4, 2013
Manufacturer
HILL-ROM, INC.
Product Code
FNL
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
TX, US
Reporter Occupation
UNKNOWN

Narratives

Additional Manufacturer Narrative · 1

THE HILL-ROM TECHNICIAN REPLACED THE HEAD UP VALVE TO RESOLVE THE ISSUE.

Description of Event or Problem · 1

THE TECHNICIAN ALLEGED THE HEAD SECTION WOULD NOT GO UP. NO INJURY REPORTED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
90240 TOTALCARE BED A/C POWERED ADJUSTABLE HOSPITAL BED FNL HILL-ROM, INC. 1900

Patients

Seq Age Sex Outcome Treatment
1