IMPLANTABLE PACEMAKER PULSE-GENERATOR

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a foreign,health professional report with the FDA on 2020-03-17 for IMPLANTABLE PACEMAKER PULSE-GENERATOR manufactured by Boston Scientific Corporation.

Event Text Entries

[183752307] As no further information concerning this report is expected, our investigation is complete. This investigation will be updated should further information be provided. (b)(4).
Patient Sequence No: 1, Text Type: N, H10


[183752308] It was reported that, during a normal device changeout procedure, the insulation on the existing right ventricular (rv) lead was damaged. Subsequently, this rv lead was capped/surgically abandoned, and another lead was successfully placed. No additional adverse patient effects were reported.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number2124215-2020-05368
MDR Report Key9842709
Report SourceFOREIGN,HEALTH PROFESSIONAL
Date Received2020-03-17
Date of Report2020-03-17
Date of Event2019-08-21
Date Mfgr Received2019-08-21
Date Added to Maude2020-03-17
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 ContactTIMOTHY DEGROOT DEGROOT
Manufacturer Street4100 HAMLINE AVENUE NORTH
Manufacturer CitySAINT PAUL MN 55112
Manufacturer CountryUS
Manufacturer Postal55112
Manufacturer Phone6515826168
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Generic NameIMPLANTABLE PACEMAKER PULSE-GENERATOR
Product CodeDXY
Date Received2020-03-17
OperatorLAY USER/PATIENT
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerBOSTON SCIENTIFIC CORPORATION
Manufacturer Address4100 HAMLINE AVENUE NORTH SAINT PAUL MN 55112 US 55112


Patients

Patient NumberTreatmentOutcomeDate
101. Hospitalization; 2. Other; 3. Required No Informationntervention 2020-03-17

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