LIGACLIP*ENDO LARGE APPLIER EL414

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2018-02-07 for LIGACLIP*ENDO LARGE APPLIER EL414 manufactured by Ethicon Endo-surgery, Llc..

Event Text Entries

[99763744] (b)(4). Device analysis: the analysis results found that the el414 device was received with no apparent damage. In an attempt to replicate the reported incident, the device was tested for functionality. Upon functional testing of the device, the instrument loaded, retained and deployed 6 clips as intended. The instrument was fully functional and conforming to our manufacturing requirements. No conclusion could be reached as to what may have caused the reported incident. The batch history records were reviewed and certed by external manufacturing that the manufacturing criteria was met prior to the release of the equipment.?
Patient Sequence No: 1, Text Type: N, H10


[99763745] It was reported that during a laparoscopic cholecystectomy, clips not closing properly from the device.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number3005075853-2018-07828
MDR Report Key7247307
Date Received2018-02-07
Date of Report2018-01-31
Date of Event2017-08-14
Date Mfgr Received2017-08-31
Device Manufacturer Date2014-02-28
Date Added to Maude2018-02-07
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 ContactMILTON GARRETT
Manufacturer Street475 CALLE C
Manufacturer CityGUAYNABO 00969
Manufacturer Postal00969
Manufacturer Phone5133378865
Manufacturer G1ETHICON ENDO-SURGERY, LLC.
Manufacturer Street475 CALLE C
Manufacturer CityGUAYNABO 00969
Manufacturer Postal Code00969
Single Use3
Previous Use Code3
Event Type3
Type of Report0

Device Details

Brand NameLIGACLIP*ENDO LARGE APPLIER
Generic NameLIGACLIP
Product CodeHBT
Date Received2018-02-07
Returned To Mfg2018-01-31
Catalog NumberEL414
OperatorHEALTH PROFESSIONAL
Device AvailabilityR
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerETHICON ENDO-SURGERY, LLC.
Manufacturer Address475 CALLE C GUAYNABO 00969 00969


Patients

Patient NumberTreatmentOutcomeDate
10 2018-02-07

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