LIGACLIP*ENDO MED/LG APPLIER EL314

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2018-05-09 for LIGACLIP*ENDO MED/LG APPLIER EL314 manufactured by Ethicon Endo-surgery, Llc..

Event Text Entries

[107832746] (b)(4). Only event year known: 2018. 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


[107832747] It was reported, clip malformation. There were no patient consequences.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number3005075853-2018-09715
MDR Report Key7498854
Date Received2018-05-09
Date of Report2018-04-18
Date Mfgr Received2018-05-11
Device Manufacturer Date2017-11-30
Date Added to Maude2018-05-09
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 MED/LG APPLIER
Generic NameLIGACLIP APPLIER
Product CodeHBT
Date Received2018-05-09
Returned To Mfg2018-05-11
Catalog NumberEL314
OperatorHEALTH PROFESSIONAL
Device AvailabilityR
Device AgeDA
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 2018-05-09

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