LIGACLIP EL414

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 2017-09-27 for LIGACLIP EL414 manufactured by Ethicon Endo-surgery, Llc..

Event Text Entries

[87890825] (b)(4). Attempts have been made to retrieve the device. To date the device has not been returned. If the device or further details are received at a later date a supplemental medwatch will be sent.
Patient Sequence No: 1, Text Type: N, H10


[87890826] It was reported that during a hepatectomy, could not close. During the endoscopic left lateral hepatectomy, the clip could not close. Changed chinese brand product to complete the procedure. There is no report on the patient's injury.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number3005075853-2017-05213
MDR Report Key6897143
Report SourceFOREIGN
Date Received2017-09-27
Date of Report2017-09-05
Date of Event2017-09-04
Date Mfgr Received2017-09-05
Date Added to Maude2017-09-27
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 Report3

Device Details

Brand NameLIGACLIP
Generic NameLIGACLIP
Product CodeHBT
Date Received2017-09-27
Catalog NumberEL414
Lot NumberNA
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by Mfgr*
Device Sequence No1
Device Event Key0
ManufacturerETHICON ENDO-SURGERY, LLC.
Manufacturer Address475 CALLE C GUAYNABO 00969 00969


Patients

Patient NumberTreatmentOutcomeDate
10 2017-09-27

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