FDA Adverse Event Malfunction Summary report: N

TOTALCARE BED

MDR report key: 2050126 · Received April 5, 2011

Report

Report Number
1824206-2011-02017
Event Type
Malfunction
Date Received
April 5, 2011
Date of Event
March 14, 2011
Report Date
March 14, 2011
Manufacturer
HILL-ROM INC.
Product Code
FNL
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
MS, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

TECHNICIAN FOUND THAT THE ACCOUNT HAS PULLED OUT THE WIRES ON THE HAND PENDANT. THE ACCOUNT HAS DECIDED TO NOT REPLACE THE PT HAND PENDANT AT THIS TIME. NO FURTHER INFO IS AVAILABLE ON THE REPAIR OF THE BED.

Description of Event or Problem · 1

ACCOUNT ALLEGED THAT WIRES ON THE PT HAND PENDANT WERE EXPOSED. NO REPORT OF INJURY.

Devices

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

Patients

Seq Age Sex Outcome Treatment
1