FDA Adverse Event Malfunction Summary report: N

TOTALCARE SPORT BED

MDR report key: 2050870 · Received April 4, 2011

Report

Report Number
1824206-2011-01995
Event Type
Malfunction
Date Received
April 4, 2011
Date of Event
March 8, 2011
Report Date
March 8, 2011
Manufacturer
HILL-ROM, INC.
Product Code
FNL
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
IL, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

THE TECHNICIAN FOUND THE HEAD UP VALVE NOT FUNCTIONING PROPERLY DUE TO THE O-RING NOT BEING ADJUSTED. THE TECHNICIAN ADJUSTED THE O-RING ON THE HEAD UP VALVE TO RESOLVE THE ISSUE.

Description of Event or Problem · 1

ACCOUNT ALLEGED THAT THE HEAD SECTION WOULD NOT GO UP AND DOWN. NO PATIENT IMPACT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 TOTALCARE SPORT BED A/C POWERED ADJUSTABLE HOSPITAL BED FNL HILL-ROM, INC. 1900

Patients

Seq Age Sex Outcome Treatment
1