FDA Adverse Event Malfunction Summary report: N

VERSACARE BED

MDR report key: 3880528 · Received May 30, 2014

Report

Report Number
1824206-2014-01679
Event Type
Malfunction
Date Received
May 30, 2014
Date of Event
May 6, 2014
Report Date
May 6, 2014
Manufacturer
HILL-ROM, INC.
Product Code
FNL
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
CA
Reporter Occupation
UNKNOWN

Narratives

Additional Manufacturer Narrative · 1

THE TECH FOUND THAT THE COMMUNICATION CABLE WAS PINCHED. THE MOST LIKELY CAUSE IS THE COMMUNICATION CABLE NOT BEING PROPERLY STOWED BEFORE THE BED WAS TRANSPORTED. PER HILL-ROM'S HEALTH HAZARD EVAL: DURING USAGE THE PINS FROM THE PORT CONNECTED TO THE FACILITY WALL SIDE MAY BECOME DAMAGED (BROKEN, BENT ETC.). THE PRIMARY ROOT CAUSE FOR THIS IS THAT THE COMMUNICATION CABLE IS NOT PROPERLY REMOVED FROM THE WALL AND SECURED TO THE BED FRAME BEFORE TRANSPORTING THE BED. WHEN THE COMMUNICATION CABLE IS PULLED FROM THE WALL AT AN ANGLE THERE IS A POTENTIAL FOR THE PINS/CONNECTOR TO GET DAMAGED. THIS IS AN INHERENT PRODUCT USE CASE ISSUE (POTENTIAL MISUSE) AND NOT A PRODUCT FAILURE TO MEET THE SPECIFIED PERFORMANCE REQUIREMENTS. NURSE CALL SYSTEMS IN ACCORDANCE WITH UL 1069 REQUIRES THAT THE NURSE CALL FUNCTION BE SUPERVISED, MEANING THAT IF FOR ANY REASON THE CIRCUIT IS INTERRUPTED A NURSE CALL OR TROUBLE SIGNAL IS SENT TO THE NURSE'S STATION. WHAT THIS MEANS IS THAT THERE IS NO WAY FOR A SIDECOM COMMUNICATION CABLE TO HAVE A BENT PIN, BROKEN WIRE OR OTHER ISSUE IN THE NURSE CALL CIRCUIT WITHOUT THE FACILITY STAFF HAVING KNOWLEDGE WITHOUT PRIOR CANCELLATION OF A NURSE CALL.

Description of Event or Problem · 1

THE ACCOUNT REPORTED THE NURSE CALL DID NOT FUNCTION. THE BED WAS LOCATED IN MAINTENANCE AT THE FACILITY. THERE WAS NO PT/USER INJURY REPORTED. THIS REPORT WAS FILED IN OUR COMPLAINT HANDLING SYSTEM AS COMPLAINT #(B)(4).

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
319897 VERSACARE BED A/C POWERED ADJUSTABLE HOSPITAL BED FNL HILL-ROM, INC. 3200

Patients

Seq Age Sex Outcome Treatment
1