FDA Adverse Event Malfunction Summary report: N

TOTALCARE

MDR report key: 2190718 · Received July 29, 2011

Report

Report Number
1824206-2011-04021
Event Type
Malfunction
Date Received
July 29, 2011
Date of Event
July 12, 2011
Report Date
July 12, 2011
Manufacturer
HILL-ROM, INC.
Product Code
FNL
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
WA, US
Reporter Occupation
UNKNOWN

Narratives

Additional Manufacturer Narrative · 1

THE TECH ISOLATED ISSUE TO THE HEAD CYLINDER. HE REPLACED THE HEAD CYLINDER TO REPAIR THE BED.

Description of Event or Problem · 1

INFO RECEIVED INDICATES THE HEAD SECTION WILL NOT GO UP OR DOWN WHEN PUSHING THE BUTTON ON THE SIDERAIL OR MANUALLY, AND THE MANUAL CPR WILL NOT WORK.

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