THERMO SCIENTIFIC FINESSE ME ELECTRONIC MICROT 77500102

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 99 report with the FDA on 2014-11-10 for THERMO SCIENTIFIC FINESSE ME ELECTRONIC MICROT 77500102 manufactured by Therno Shandon Limited (trading As Thermo Fisher Scientific).

Event Text Entries

[5235005] On (b)(6) 2014, a hospital lab in (b)(6) reported to (b)(6) the following: a female lab technician was operating a finesse me microtome (sn (b)(4)). She thought she pressed the stop button, and placed her right hand near the blade. The machine advanced and sliced off part of her finger near the fingernail. She went to the er and the tissue that was cut-off could not be reattached. She was released from the er and went back to work, but later went home due to her finger hurting. The employee spoken to by (b)(6) was from the hospitals biomet/safety department, not the female lab technician. The hospital also reported that they tested the machine "about a 100 times" and could not replicate the issue. The hospital formalized this report to thermo fisher scientific via (b)(6) using mandatory fda 3500a reporting form (appendix 3 8415 medwatch finesse microtome). On (b)(6) 2014, the hospital confirmed the following: "starting with the first block of the day, when switching from the trim mode to the section mode, the user had hit the run button to stop the microtome. She was grabbing for a ribbon but the machine had not stopped and she cut her finger". The root cause was determined as user error. Investigations into the functioning of the instrument suggests the instrument operated as intended. The scenario reported could not be repeated. The only hypothesis for the cause of the incident the user did not depresses the "run" button the second time as thought, thus the instrument did not stop and in continuing its intended operation the user cut their finger. A review of the instrument by the hospitals biomedical engineer showed the instrument operated as intended. Currently the hospital outsources the servicing of the instrument. This outsourcing is tasked independently of thermo fisher scientific. However as a result of the reported incident a usa thermo fisher service technician visited the hospital, the purpose of this visit was to ensure there were no faults in the operation of the instrument that would cause or contribute to the cut finger. The instrument was found to be working as intended and the thermo field service engineer could not recreate the incident as described.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1831638-2014-00001
MDR Report Key4360604
Report Source99
Date Received2014-11-10
Date of Report2014-11-03
Date of Event2014-10-13
Date Facility Aware2014-10-13
Report Date2014-11-07
Date Reported to FDA2014-11-10
Date Reported to Mfgr2014-10-15
Date Added to Maude2014-12-29
Event Key0
Report Source CodeDistributor report
Manufacturer LinkN
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Reporter OccupationBIOMEDICAL ENGINEER
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer Street4481 CAMPUS DR.
Manufacturer CityKALAMAZOO MI 49008
Manufacturer CountryUS
Manufacturer Postal49008
Manufacturer G1RICHARD-ALLAN SCIENTIFIC
Manufacturer Street4481 CAMPUS DR.
Manufacturer CityKALAMAZOO MI 49008
Manufacturer CountryUS
Manufacturer Postal Code49008
Single Use0
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameTHERMO SCIENTIFIC FINESSE ME ELECTRONIC MICROT
Generic NameFINESSE ME
Product CodeIDO
Date Received2014-11-10
Catalog Number77500102
OperatorHEALTH PROFESSIONAL
Device AvailabilityY
Device Age11 YR
Device Eval'ed by Mfgr*
Device Sequence No1
Device Event Key0
ManufacturerTHERNO SHANDON LIMITED (TRADING AS THERMO FISHER SCIENTIFIC)
Manufacturer AddressRUNCORN, CHESHIRE WA71TA UK WA7 1TA


Patients

Patient NumberTreatmentOutcomeDate
101. Hospitalization 2014-11-10

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