FDA Adverse Event Malfunction Summary report: N

TOTALCARE PULMONARY SURFACE

MDR report key: 1843732 · Received September 21, 2010

Report

Report Number
1824206-2010-10048
Event Type
Malfunction
Date Received
September 21, 2010
Date of Event
August 26, 2010
Report Date
August 26, 2010
Manufacturer
HILL-ROM, INC.
Product Code
FNL
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
NY, US
Reporter Occupation
UNKNOWN

Narratives

Additional Manufacturer Narrative · 1

TECHNICIAN CHECKED THE SPRING LATCH AND PIN LATCH AND THEY WERE DIRTY. TECHNICIAN CLEANED AND LUBRICATED THE LATCHES TO RESOLVE THE ISSUE.

Description of Event or Problem · 1

TECHNICIAN ALLEGED THAT TWO SIDE RAILS, THE LEFT FOOT AND THE RIGHT HEAD, WERE NOT LOCKED.

Devices

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

Patients

Seq Age Sex Outcome Treatment
1