FDA Adverse Event Malfunction Summary report: N

VERSACARE BED

MDR report key: 2050489 · Received March 15, 2011

Report

Report Number
1824206-2011-01556
Event Type
Malfunction
Date Received
March 15, 2011
Date of Event
February 18, 2011
Report Date
February 18, 2011
Manufacturer
HILL-ROM INC.
Product Code
FNL
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
WA, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

THE TECHNICIAN FOUND THE BED HAD NO FUNCTIONS AND A NETWORK HEARTBEAT FAILURE DUE TO A SHORTED COILED CABLE. HE REPLACED THE LEFT COILED CABLE, THE POWER SUPPLY BOARD, SCALE BOARD, LOGIC BOARD; MOTOR CONTROL BOARD AND THE LEFT HEAD OBSTACLE DETECT TO REPAIR THE BED.

Description of Event or Problem · 1

INFO REC'D INDICATES THE LEFT COILED CABLE WAS CUT, EXPOSING BARE METAL WIRING. THIS ALSO CAUSED THE POWER SUPPLY BOARD, SCALE BOARD, LOGIC BOARD, MOTOR CONTROL BOARD AND THE LEFT HEAD OBSTACLE DETECT TO SHORT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 VERSACARE BED AC-POWERED ADJUSTABLE HOSPITAL BED FNL HILL-ROM INC. 3200

Patients

Seq Age Sex Outcome Treatment
1