NANOKNIFE SYSTEM 20300101

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a foreign report with the FDA on 2018-03-01 for NANOKNIFE SYSTEM 20300101 manufactured by Angiodynamics.

Event Text Entries

[101240564] It was reported that the nanoknife system ((b)(4) ) involved in the incident is available to be returned to the manufacturer for evaluation. To date, the generator has yet to be returned. Attempts are being made to obtain the unit. The results of the unit evaluation will be sent via a follow up medwatch. (b)(4).
Patient Sequence No: 1, Text Type: N, H10


[101240565] As reported to angiodynamics on (b)(6) 2018, the treating physician reported that the irreversible electroporation (ire) generator shut down approximately 5-6 times during an ire procedure. As a result, the treatment is prolonged approximately 90 minutes longer than as normally performed. During this time, the patient is under anesthesia. It was reported that the patient suffered no adverse effects due to the event. The customer has requested the facility's unit be evaluated by the manufacturer. The unit has yet to be returned to the manufacturer for evaluation.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1319211-2018-00018
MDR Report Key7305633
Report SourceFOREIGN
Date Received2018-03-01
Date of Report2018-06-12
Date of Event2018-02-07
Date Mfgr Received2018-02-07
Date Added to Maude2018-03-01
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactLAW RYAN
Manufacturer Street10 GLENS FALLS TECHNICAL PARK
Manufacturer CityGLENS FALLS NY 12801
Manufacturer CountryUS
Manufacturer Postal12801
Manufacturer Phone5187424488
Manufacturer G1ANGIODYNAMICS
Manufacturer Street10 GLENS FALLS TECHNICAL PARK
Manufacturer CityGLENS FALLS NY 12801
Manufacturer CountryUS
Manufacturer Postal Code12801
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameNANOKNIFE SYSTEM
Generic NameLOW ENERGY DIRECT CURRENT ABLATION SYSTEM
Product CodeOAB
Date Received2018-03-01
Returned To Mfg2018-02-14
Model Number20300101
OperatorPHYSICIAN
Device AvailabilityR
Device AgeDA
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerANGIODYNAMICS
Manufacturer Address603 QUEENSBURY AVENUE QUEENSBURY NY 12804 US 12804


Patients

Patient NumberTreatmentOutcomeDate
101. Required No Informationntervention 2018-03-01

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