FDA Adverse Event Malfunction Summary report: N

TOTALCARE

MDR report key: 2151387 · Received June 8, 2011

Report

Report Number
1824206-2011-03148
Event Type
Malfunction
Date Received
June 8, 2011
Date of Event
May 19, 2011
Report Date
May 19, 2011
Manufacturer
HILL-ROM INC.
Product Code
FNL
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
FL, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

TECHNICIAN FOUND THE BED IN STORAGE AREA. FOOT HI/LO DRIFTING DOWN. CLEANED VALVE AND CHECKED FOR DAMAGE. REINSTALLED VALVE TO RESOLVE THIS ISSUE.

Description of Event or Problem · 1

INFO RECEIVED INDICATED THAT THE FOOT HI/LO WAS DRIFTING DOWN. NO INJURIES 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