FDA Adverse Event Malfunction Summary report: N

TOTAL CARE BED

MDR report key: 3033280 · Received March 1, 2013

Report

Report Number
1824206-2013-01179
Event Type
Malfunction
Date Received
March 1, 2013
Date of Event
February 1, 2013
Report Date
February 1, 2013
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 REPLACED THE HEAD UP VALVE TO RESOLVE THE ISSUE.

Description of Event or Problem · 1

THE TECHNICIAN ALLEGED THAT THE HEAD OF THE BED WILL NOT RAISE. NO PATIENT IMPACT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
90678 TOTAL CARE BED A/C POWERED ADJUSTABLE HOSPITAL BED FNL HILL-ROM, INC. 1900

Patients

Seq Age Sex Outcome Treatment
1