LEAD MODEL 302 302-20

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative report with the FDA on 2020-03-20 for LEAD MODEL 302 302-20 manufactured by Cyberonics - Houston.

Event Text Entries

[188027859] During a periodic review of the programming history database it was seen that patient has high lead impedance and low output current on their device. No explant has been reported to date. No additional relevant information has been received to date.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1644487-2020-00472
MDR Report Key9862790
Report SourceCOMPANY REPRESENTATIVE
Date Received2020-03-20
Date of Report2020-03-20
Date of Event2012-10-22
Date Mfgr Received2020-02-24
Device Manufacturer Date2008-06-24
Date Added to Maude2020-03-20
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 G1CYBERONICS - HOUSTON
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 NameLEAD MODEL 302
Generic NameLEAD
Product CodeLYJ
Date Received2020-03-20
Model Number302-20
Lot Number200841
Device Expiration Date2011-06-24
OperatorLAY USER/PATIENT
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerCYBERONICS - HOUSTON
Manufacturer Address100 CYBERONICS BLVD HOUSTON TX 77058 US 77058


Patients

Patient NumberTreatmentOutcomeDate
10 2020-03-20

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