TRANSVENOUS LEAD 401652

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 2018-10-30 for TRANSVENOUS LEAD 401652 manufactured by Mpri.

Event Text Entries

[125495076] If information is provided in the future, a supplemental report will be issued.
Patient Sequence No: 1, Text Type: N, H10


[125495077] It was reported that the implantable pulse generator (ipg) and leads were removed due to infection. The system will be replaced in the future. No further patient complications have been reported as a result of this event.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number2649622-2018-17698
MDR Report Key8019898
Report SourceCOMPANY REPRESENTATIVE,HEALTH
Date Received2018-10-30
Date of Report2018-10-30
Date of Event2018-10-02
Date Mfgr Received2018-10-02
Date Added to Maude2018-10-30
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 ContactANNE SCHILLING
Manufacturer Street8200 CORAL SEA ST NE
Manufacturer CityMOUNDS VIEW MN 55112
Manufacturer CountryUS
Manufacturer Postal55112
Manufacturer Phone7635052036
Manufacturer G1MPRI
Manufacturer StreetROAD 149 KM 56.3
Manufacturer CityVILLALBA PR 00766
Manufacturer CountryUS
Manufacturer Postal Code00766
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameTRANSVENOUS LEAD
Generic NameADAPTOR, LEAD, PACEMAKER
Product CodeDTD
Date Received2018-10-30
Model Number401652
Catalog Number401652
OperatorLAY USER/PATIENT
Device AvailabilityN
Device Eval'ed by Mfgr*
Device Sequence No1
Device Event Key0
ManufacturerMPRI
Manufacturer AddressROAD 149 KM 56.3 VILLALBA PR 00766 US 00766


Patients

Patient NumberTreatmentOutcomeDate
101. Hospitalization; 2. Required No Informationntervention 2018-10-30

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