CHALGREN 242-637-24TP-1

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2018-06-15 for CHALGREN 242-637-24TP-1 manufactured by Chalgren Enterprises, Inc..

Event Text Entries

[111310012] Chalgren was unaware of the reported incident prior to receiving medwatch notification by mail. Upon receiving information on 05/15/2018, chalgren contacted the initial reporter same day by phone and email to initiate the investigation and response. Priority was made to gather additional investigational information regarding incident. Initial response indicated that there was no additional information available other than what had been initially reported. The information provided in the initial report was taken directly from the reporting facilities incident report. It was reported back to chalgren by the facility director of risk management that the reporting facility was a teaching hospital, and that the incident may have been a technique issue on behalf of the resident performing the procedure. Attempts at gathering additional information regarding the actual incident were unable to achieve any results. Chalgren was informed on 05/22/2018 that the needle was available for return and so it was requested to return the device for evaluation. Device was received by chalgren on 06/08/2018. Only hub and leadwire assembly were returned - the actual needle was not included. Evaluation and examination on 06/11/2018 by chalgren determined that the base of the needle was still intact within the hub assembly and that needle appears to have broken off just above the hub. Initial testing on identical needle hub assemblies demonstrates that to achieve this result would require bending of the needle at a 90 degree angle just above the needle hub junction after deep insertion, and then bending it back 90 degrees in the opposite direction in an attempt to straighten or remove the needle. This action puts abnormal stress on the needle causing it to fail and break as seen in the returned device. As there is no further information available from the reporting facility, this incident is being attributed to user error.
Patient Sequence No: 1, Text Type: N, H10


[111310013] Report by customer that needle from injectable monopolar needle electrode broke off in patient while patient was receiving botox injections for spasticity. Needle was reported to break off in "patient muscle", exact location not reported. Report states that acute care surgery was called in to identify the needle via ultrasound and was able to extract the needle.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number2939713-2018-00001
MDR Report Key7608112
Date Received2018-06-15
Date of Report2018-06-15
Date of Event2018-05-01
Date Mfgr Received2018-05-15
Device Manufacturer Date2018-02-16
Date Added to Maude2018-06-15
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Reporter OccupationRISK MANAGER
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactMR. ANDREW FIGUEROA
Manufacturer Street380 TOMKINS CT
Manufacturer CityGILROY CA 95020
Manufacturer CountryUS
Manufacturer Postal95020
Manufacturer Phone4088473994
Single Use3
Previous Use Code3
Event Type3
Type of Report0

Device Details

Brand NameCHALGREN
Generic NameELECTRODE, NEEDLE, DIAGNOSTIC ELECTROMYOGRAPH
Product CodeIKT
Date Received2018-06-15
Model Number242-637-24TP-1
Lot NumberB288
OperatorPHYSICIAN
Device AvailabilityN
Device Eval'ed by MfgrN
Device Sequence No1
Device Event Key0
ManufacturerCHALGREN ENTERPRISES, INC.
Manufacturer Address380 TOMKINS CT GILROY CA 95020 US 95020


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2018-06-15

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