FDA Adverse Event Malfunction Summary report: N

TOTALCARE

MDR report key: 1964124 · Received December 21, 2010

Report

Report Number
1824206-2010-11845
Event Type
Malfunction
Date Received
December 21, 2010
Date of Event
December 2, 2010
Report Date
December 2, 2010
Manufacturer
HILL-ROM INC.
Product Code
FNL
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
SC, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

TECHNICIAN ASKED ACCOUNT TO ISOLATE THE COIL AND THEN THE VALVES. NO FURTHER INFO IS AVAILABLE ON THE REPAIR OF THIS BED AT THIS TIME.

Description of Event or Problem · 1

ACCOUNT ALLEGES, THE HEAD SECTION WILL NOT RAISE. THERE WAS NO REPORTED INJURY OR INCIDENT.

Devices

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

Patients

Seq Age Sex Outcome Treatment
1