FDA Adverse Event Malfunction Summary report: N

TOTALCARE

MDR report key: 2072059 · Received April 21, 2011

Report

Report Number
1824206-2011-02320
Event Type
Malfunction
Date Received
April 21, 2011
Date of Event
March 29, 2011
Report Date
March 29, 2011
Manufacturer
HILL-ROM, INC.
Product Code
FNL
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
NJ, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

THE ENGINEER CHECKED FOR MAGNETIC PULL ON THE VALVE AND THE HEAD SECTION WENT UP. THE ACCOUNT DID NOT IDENTIFY A CAUSE, POSSIBLE LOOSE CONNECTION.

Description of Event or Problem · 1

THE ACCOUNT ALLEGED THE HEAD OF THE BED WILL NOT RISE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 TOTALCARE AC-POWERED ADJUSTABLE HOSPITAL BED FNL HILL-ROM, INC. 1900

Patients

Seq Age Sex Outcome Treatment
1