FDA Adverse Event Malfunction Summary report: N

TOTALCARE

MDR report key: 2170787 · Received June 22, 2011

Report

Report Number
1824206-2011-03382
Event Type
Malfunction
Date Received
June 22, 2011
Date of Event
June 6, 2011
Report Date
June 6, 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 BED SHOP. PROBLEM: NO HEAD FUNCTION DUE TO STUCK VALVES. REPLACED STUCK VALVES TO RESOLVE THIS ISSUE.

Description of Event or Problem · 1

FACILITY REQUESTED SERVICE TECHNICIAN TO MAKE REPAIRS TO THIS BED DUE TO ISSUE WITH THE HYDRAULICS. NO FURTHER DESCRIPTION OF ISSUE. NO PT IMPACT.

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