GENERATOR MODEL 102

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,health report with the FDA on 2019-12-10 for GENERATOR MODEL 102 manufactured by Livanova Usa, Inc..

Event Text Entries

[170119648] Patient referred for device explant due to the device migrating towards the patient's left breast as well as the device causing pain. No known surgical intervention has occurred to date. No other relevant information has been received to date.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1644487-2019-02382
MDR Report Key9446580
Report SourceCOMPANY REPRESENTATIVE,HEALTH
Date Received2019-12-10
Date of Report2020-02-26
Date of Event2019-10-24
Date Mfgr Received2020-02-11
Device Manufacturer Date2005-09-09
Date Added to Maude2019-12-10
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 ContactMRS. RACHEL KOHN
Manufacturer Street100 CYBERONICS BLVD SUITE 600
Manufacturer CityHOUSTON TX 77058
Manufacturer CountryUS
Manufacturer Postal77058
Manufacturer Phone2812287200
Manufacturer G1LIVANOVA USA, INC.
Manufacturer Street100 CYBERONICS BLVD SUITE 600
Manufacturer CityHOUSTON TX 77058
Manufacturer CountryUS
Manufacturer Postal Code77058
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameGENERATOR MODEL 102
Generic NameGENERATOR
Product CodeMUZ
Date Received2019-12-10
Model Number102
Lot Number013894
Device Expiration Date2007-07-21
OperatorLAY USER/PATIENT
Device AvailabilityN
Device AgeDA
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerLIVANOVA USA, INC.
Manufacturer Address100 CYBERONICS BLVD HOUSTON TX 77058 US 77058


Patients

Patient NumberTreatmentOutcomeDate
101. Required No Informationntervention 2019-12-10

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