ICEFORCE 2.1 CX 90? CRYOABLATION NEEDLE FPRPR3602

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,health report with the FDA on 2020-03-18 for ICEFORCE 2.1 CX 90? CRYOABLATION NEEDLE FPRPR3602 manufactured by Galil Medical Ltd..

Event Text Entries

[184348545] Five iceforce needles were tested and used in a cryoablation procedure. During the first thaw cycle when activating fastthaw, the patient began to twitch. The needles were turned on and off separately to isolate which needle was causing the issue. A passive thaw was used on the faulty needle for the remainder of the case. The case completed with no injury to the patient. The defective needle will be returned to the manufacturer for investigation.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number9616793-2020-00063
MDR Report Key9851187
Report SourceCOMPANY REPRESENTATIVE,HEALTH
Date Received2020-03-18
Date of Report2020-03-18
Date of Event2020-02-17
Date Mfgr Received2020-02-17
Date Added to Maude2020-03-18
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 ContactMS. SANDRA BAUSBACK-ABALLO
Manufacturer Street300 CONSHOHOCKEN STATE RD, 300 FOUR FALLS CORPORATE CTR.
Manufacturer CityWEST CONSHOHOCKEN, PA
Manufacturer CountryUS
Manufacturer Phone3311537
Manufacturer G1GALIL MEDICAL LTD.
Manufacturer Street1 TAVOR BUILDING PO BOX 224, INDUSTRIAL PARK
Manufacturer CityYOKNEAM, 2069203
Manufacturer CountryIS
Manufacturer Postal Code2069203
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameICEFORCE 2.1 CX 90? CRYOABLATION NEEDLE
Generic NameCRYOABLATION NEEDLE
Product CodeGEH
Date Received2020-03-18
Model NumberFPRPR3602
Catalog NumberFPRPR3602
OperatorHEALTH PROFESSIONAL
Device AvailabilityY
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerGALIL MEDICAL LTD.
Manufacturer Address1 TAVOR BUILDING P.O. BOX 224, INDUSTRIAL PARK YOKNEAM, 2069203 IS 2069203


Patients

Patient NumberTreatmentOutcomeDate
10 2020-03-18

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