8CH INFINITY DBS FLEX EXTN KIT, 50CM, B 6371

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,foreig report with the FDA on 2020-03-27 for 8CH INFINITY DBS FLEX EXTN KIT, 50CM, B 6371 manufactured by St. Jude Medical - Neuromodulation.

Event Text Entries

[185324909] The results/method and conclusion codes along with investigation results will be provided in the final report.
Patient Sequence No: 1, Text Type: N, H10


[185324910] Related manufacturer reference number: 1627487-2020-03341. It was reported that prior to elective ipg replacement procedure on (b)(6) 2020, patient? S right lead showed high lead impedance values. During procedure, after opening ipg pocket it was found out that patient has a twiddler? S syndrome and hence lead and extension are wrapped up around each other. It was also noticed that right lead had migrated.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1627487-2020-03342
MDR Report Key9891606
Report SourceCOMPANY REPRESENTATIVE,FOREIG
Date Received2020-03-27
Date of Report2020-03-27
Date of Event2020-03-06
Date Mfgr Received2020-03-06
Device Manufacturer Date2016-07-25
Date Added to Maude2020-03-27
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 ContactANDREA DEITZ
Manufacturer Street6901 PRESTON ROAD
Manufacturer CityPLANO TX 75024
Manufacturer CountryUS
Manufacturer Postal75024
Manufacturer Phone9723098000
Manufacturer G1ST. JUDE MEDICAL - NEUROMODULATION
Manufacturer Street6901 PRESTON RD
Manufacturer CityPLANO TX 75024
Manufacturer CountryUS
Manufacturer Postal Code75024
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand Name8CH INFINITY DBS FLEX EXTN KIT, 50CM, B
Generic NameDBS EXTENSION
Product CodeMHY
Date Received2020-03-27
Model Number6371
Catalog Number6371
Lot Number5577940
Device Expiration Date2018-07-25
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerST. JUDE MEDICAL - NEUROMODULATION
Manufacturer Address6901 PRESTON RD PLANO TX 75024 US 75024


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2020-03-27

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