ACCOLADE SR L300

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a health professional report with the FDA on 2020-03-30 for ACCOLADE SR L300 manufactured by Boston Scientific Corporation.

Event Text Entries

[185761710] No further information is available at this time. This report will be updated should further information become available.
Patient Sequence No: 1, Text Type: N, H10


[185761711] It was reported that this pacemaker exhibited oversensing of the atrial channel in which the minute ventilation feature was disabled. The electrogram revealed the oversensing led to pacing inhibition in this pacing dependent patient. This pacemaker remains in service. No adverse patient effects were reported.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number2124215-2020-04132
MDR Report Key9901573
Report SourceHEALTH PROFESSIONAL
Date Received2020-03-30
Date of Report2020-03-30
Date of Event2019-10-16
Date Mfgr Received2020-03-04
Device Manufacturer Date2018-03-04
Date Added to Maude2020-03-30
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Reporter OccupationOTHER HEALTH CARE PROFESSIONAL
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactTIMOTHY DEGROOT
Manufacturer Street4100 HAMLINE AVENUE NORTH
Manufacturer CitySAINT PAUL MN 55112
Manufacturer CountryUS
Manufacturer Postal55112
Manufacturer Phone6515826168
Manufacturer G1BOSTON SCIENTIFIC CORPORATION
Manufacturer StreetCASHEL ROAD
Manufacturer CityCLONMEL
Manufacturer CountryEI
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameACCOLADE SR
Generic NameIMPLANTABLE DEVICE
Product CodeLWP
Date Received2020-03-30
Model NumberL300
Catalog NumberL300
Lot Number721297
Device Expiration Date2020-02-14
OperatorLAY USER/PATIENT
Device AvailabilityN
Device AgeDA
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
10 2020-03-30

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