LIGASURE ADVANCE PISTOL GRIP LF5544

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2016-05-19 for LIGASURE ADVANCE PISTOL GRIP LF5544 manufactured by Covidien Lp.

Event Text Entries

[46034202] Covidien reference # (b)(4). Date of initial report: 05/19/2016. To date the incident sample has not been received for evaluation. If the sample is received or if additional information pertinent to the incident is obtained a follow-up report will be submitted.
Patient Sequence No: 1, Text Type: N, H10


[46034203] The customer reported that the clear insulation near the device jaws was coming off and the device wasn't activating correctly. There was no patient injury as a result of the reported condition.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1717344-2016-00429
MDR Report Key5666281
Date Received2016-05-19
Date of Report2016-05-13
Date Mfgr Received2016-05-13
Device Manufacturer Date2015-07-01
Date Added to Maude2016-05-19
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 ContactSHARON MURPHY
Manufacturer Street5920 LONGBOW DRIVE
Manufacturer CityBOULDER CO 80301
Manufacturer CountryUS
Manufacturer Postal80301
Manufacturer Phone2034925267
Single Use3
Previous Use Code3
Event Type3
Type of Report0

Device Details

Brand NameLIGASURE ADVANCE PISTOL GRIP
Generic NameLIGASURE VESSEL SEALING SYSTEM
Product CodeBWA
Date Received2016-05-19
Model NumberLF5544
Catalog NumberLF5544
Lot Number51690017X
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerCOVIDIEN LP
Manufacturer Address5920 LONGBOW DRIVE BOULDER CO 80301 US 80301


Patients

Patient NumberTreatmentOutcomeDate
10 2016-05-19

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