FDA Adverse Event Injury Summary report: N

FREEDOM EVO-2 200 MCA

MDR report key: 3504644 · Received November 19, 2013

Report

Report Number
1037985-2013-00002
Event Type
Injury
Date Received
November 19, 2013
Date of Event
November 1, 2013
Report Date
November 15, 2013
Manufacturer
TECAN SCHWEIZ
Product Code
JQW
Adverse Event
Yes
Report Source
Distributor report
Reporter Location
CA, US
Reporter Occupation
OTHER HEALTH CARE PROFESSIONAL

Narratives

Description of Event or Problem · 1

LABORATORY CALLED TECAN ON (B)(6) TO REPORT THAT DURING A TEST RUN OF AN EVO 200 MCA LIQUID HANDLING PIPETTOR INSTRUMENT, THE OPERATOR HAD PRESSED THE PAUSE BUTTON AND REACHED INSIDE THE INSTRUMENT TO REMOVE TIPS THAT WERE STUCK TO THE MCA HEAD. THE PAUSE BUTTON WAS LIT INDICATING INSTRUMENT WAS PAUSED. WHILE THE OPERATOR'S HAND WAS INSIDE THE INSTRUMENT, THE MCA HEAD MOVED DOWN PINNING THE OPERATOR'S HAND TO THE DECK OF THE INSTRUMENT. THE OPERATOR HIT THE PAUSE BUTTON TO UNPAUSE THE INSTRUMENT AND THE MCA HEAD MOVED UP FREEING THE OPERATOR'S HAND. THE OPERATOR SUSTAINED MINOR INJURY TO THE HAND INCLUDING A CUT WITH BLEEDING. NO MEDICAL TREATMENT WAS REQUIRED OTHER THAN BASIC FIRST AID. THE TEST RUN WAS WITHOUT REAGENTS AND THE TIPS WERE CLEAN AND STERILE. NO RISK OF BIOHAZARD EXPOSURE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
598040 FREEDOM EVO-2 200 MCA PIPETTING STATION FOR CLINICAL USE JQW TECAN SCHWEIZ

Patients

Seq Age Sex Outcome Treatment
1 Other