FDA Adverse Event Malfunction Summary report: N

TOTALCARE

MDR report key: 2212145 · Received July 8, 2011

Report

Report Number
1824206-2011-03625
Event Type
Malfunction
Date Received
July 8, 2011
Date of Event
June 27, 2011
Report Date
June 30, 2011
Manufacturer
HILL-ROM, INC.
Product Code
FNL
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
CA, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

TECHNICIAN FOUND THE BED IN BASEMENT. HEAD ELEVATION HAD SLOW DRIFT. REPLACED THE VALVES TO RESOLVE THIS ISSUE.

Description of Event or Problem · 1

COMPLAINT REPORTED THAT THE EBD HAD A SLOW HEAD DOWN DRIFT. NO INJURY ALLEGED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 TOTALCARE AC-POWERED ADJUSTABLE HOSPITAL BED FNL HILL-ROM, INC. P1900

Patients

Seq Age Sex Outcome Treatment
1