FDA Adverse Event Malfunction Summary report: N

CAREASSIST BED

MDR report key: 1880032 · Received October 18, 2010

Report

Report Number
3006697241-2010-00026
Event Type
Malfunction
Date Received
October 18, 2010
Date of Event
September 23, 2010
Report Date
September 23, 2010
Manufacturer
HILL-ROM DE MEXICO S DE RL DE CV
Product Code
FNL
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
IL, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

THE ACCOUNT REPLACED BOTH THE CAREGIVER AND PATIENT SIDERAIL MEMBRANES TO REPAIR THE BED.

Description of Event or Problem · 1

THE ACCOUNT ALLEGED THE BED WILL NOT SEND A NURSE CALL. THE ACCOUNT HAS REPLACED THE COMMUNICATION CABLE AND TAKEN THE BED TO ANOTHER ROOM, BUT THE ISSUE REMAINS. THE ACCOUNT INDICATED WITH THE RIGHT SIDERAIL UNPLUGGED THE BED WILL SEND A NURSE CALL FROM THE LEFT SIDERAIL AND PENDANT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 CAREASSIST BED AC POWERED HOSPITAL BED FNL HILL-ROM DE MEXICO S DE RL DE CV 1170

Patients

Seq Age Sex Outcome Treatment
1