FDA Adverse Event Injury Summary report: N

MAQUET SAS

MDR report key: 3080838 · Received April 9, 2013

Report

Report Number
3008355164-2013-00076
Event Type
Injury
Date Received
April 9, 2013
Date of Event
February 22, 2013
Report Date
February 28, 2013
Manufacturer
MAQUET SAS
Product Code
FTD
Adverse Event
Yes
Report Source
Distributor report
Reporter Location
EI
Reporter Occupation
OTHER HEALTH CARE PROFESSIONAL

Narratives

Description of Event or Problem · 1

THE HOSPITAL REPORTED THAT, WHEN THE MAIN LIGHT WAS BEING MOVED INTO A NEW POSITION, THE WHOLE LIGHT FELL ONTO A MIDWIFE AND PT, WHO WAS ON THE OPERATING THEATER TABLE. THE MIDWIFE AND PT REC'D BRUISING. (B)(4).

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
148262 MAQUET SAS FTD MAQUET SAS HANAULUX 2000 NA

Patients

Seq Age Sex Outcome Treatment
1 NI Other