FDA Adverse Event Other Summary report: N

CERETOM (TRANSFER SCAN BOARD)

MDR report key: 1315824 · Received February 13, 2009

Report

Report Number
3004938766-2009-00001
Event Type
Other
Date Received
February 13, 2009
Date of Event
October 13, 2008
Report Date
November 10, 2008
Manufacturer
NEUROLOGICA CORPORATION
Product Code
JAK
Report Source
Manufacturer report
Reporter Location
MA, US
Reporter Occupation
OTHER HEALTH CARE PROFESSIONAL

Narratives

Additional Manufacturer Narrative · 1

IMPROPER POSITIONING OF SCAN TRANSFER BOARD ONTO STRETCHER BED. WARNING LABEL WITH PROPER POSITIONING INSTRUCTIONS ARE BEING ADDED TO THE TRANSFER BOARD.

Description of Event or Problem · 1

A RADIATION TECHNICIAN SUFFERED A LEG BRUISE WHEN A PT WAS POSITIONED ONTO A TRANSFER SCAN BOARD CAUSING THE STRETCHER BED TO TIP. THE BOTTOM OF THE SCAN BOARD CAME IN CONTACT WITH TECHNOLOGIST'S LEG.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 CERETOM (TRANSFER SCAN BOARD) TRANSFER SCAN BOARD JAK NEUROLOGICA CORPORATION 1-NL3000 NA

Patients

Seq Age Sex Outcome Treatment
1 NA