FDA Adverse Event Malfunction Summary report: N

TOTALCARE BED

MDR report key: 2063860 · Received April 12, 2011

Report

Report Number
1824206-2011-02124
Event Type
Malfunction
Date Received
April 12, 2011
Date of Event
March 21, 2011
Report Date
March 21, 2011
Manufacturer
HILL-ROM, INC.
Product Code
FNL
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
FL, US
Reporter Occupation
UNKNOWN

Narratives

Additional Manufacturer Narrative · 1

TECHNICIAN FOUND THE HYDRAULIC VALVE SOLENOID FOR THE HEAD UP IS STUCK. THE TECHNICIAN REPLACED THE HYDRAULIC VALVE SOLENOID FOR THE HEAD UP TO RESOLVE THE ISSUE.

Description of Event or Problem · 1

TECHNICIAN ALLEGED THAT THE HEAD OF THE BED WILL NOT GO UP. NO PATIENT IMPACT.

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