FDA Adverse Event Malfunction Summary report: N

TOTALCARE BARIATRIC

MDR report key: 2143520 · Received June 2, 2011

Report

Report Number
1824206-2011-03048
Event Type
Malfunction
Date Received
June 2, 2011
Date of Event
March 3, 2011
Report Date
March 3, 2011
Manufacturer
HILL-ROM INC.
Product Code
FNL
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
MD, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

THE TECHNICIAN REPLACED THE COIL SOLENOID TO RESOLVE THE ISSUE.

Description of Event or Problem · 1

INFO REC'D INDICATES THE HEAD SECTION WOULD NOT LOWER PREVENTING THE BED FROM GOING INTO CPR POSITION.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 TOTALCARE BARIATRIC A/C POWERED ADJUSTABLE HOSPITAL BED FNL HILL-ROM INC. 1840

Patients

Seq Age Sex Outcome Treatment
1