ASSURITY MRI PM2272

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 2020-03-30 for ASSURITY MRI PM2272 manufactured by St. Jude Medical, Inc.(crm-sunnyvale).

Event Text Entries

[185717865] 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


[185717866] It was reported that the pacemaker had eroded through the skin. There was no sign of infection. The whole system was explanted and a new system was implanted on the right side. The patient was stable before, during and after the procedure.
Patient Sequence No: 1, Text Type: D, B5


[188152320] Analysis was normal. No anomalies were found.
Patient Sequence No: 1, Text Type: N, H10


MAUDE Entry Details

Report Number2938836-2020-02326
MDR Report Key9901665
Report SourceCOMPANY REPRESENTATIVE,HEALTH
Date Received2020-03-30
Date of Report2020-03-30
Date of Event2020-03-13
Date Mfgr Received2020-03-13
Device Manufacturer Date2019-04-04
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
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactELIZABETH BOLTZ
Manufacturer Street15900 VALLEY VIEW COURT
Manufacturer CitySYLMAR CA 91342
Manufacturer CountryUS
Manufacturer Postal91342
Manufacturer G1ST. JUDE MEDICAL, INC.(CRM-SUNNYVALE)
Manufacturer Street645 ALMANOR AVENUE
Manufacturer CitySUNNYVALE CA 94085
Manufacturer CountryUS
Manufacturer Postal Code94085
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameASSURITY MRI
Generic NameIMPLANTABLE PACEMAKER PULSE GENERATOR
Product CodeLWP
Date Received2020-03-30
Returned To Mfg2020-03-23
Model NumberPM2272
Catalog NumberPM2272
Lot NumberA000077672
OperatorHEALTH PROFESSIONAL
Device AvailabilityR
Device Eval'ed by MfgrN
Device Sequence No1
Device Event Key0
ManufacturerST. JUDE MEDICAL, INC.(CRM-SUNNYVALE)
Manufacturer Address645 ALMANOR AVENUE SUNNYVALE CA 94085 US 94085


Patients

Patient NumberTreatmentOutcomeDate
101. Required No Informationntervention 2020-03-30

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