ZINGER GUIDE WIRE - CRDM LVZRXT180S

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 2018-08-27 for ZINGER GUIDE WIRE - CRDM LVZRXT180S manufactured by Medtronic, Inc.

Event Text Entries

[118560130] If information is provided in the future, a supplemental report will be issued.
Patient Sequence No: 1, Text Type: N, H10


[118560131] It was reported that during the implant procedure, the guidewire became stuck to the tip of the left ventricular (lv) lead. The lv lead and guidewire were replaced. No patient complications have been reported as a result of this event.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1220452-2018-00105
MDR Report Key7820152
Report SourceCOMPANY REPRESENTATIVE,FOREIG
Date Received2018-08-27
Date of Report2018-08-27
Date of Event2018-08-02
Date Mfgr Received2018-08-02
Device Manufacturer Date2015-09-21
Date Added to Maude2018-08-27
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 ContactANNE SCHILLING
Manufacturer Street8200 CORAL SEA ST NE
Manufacturer CityMOUNDS VIEW MN 55112
Manufacturer CountryUS
Manufacturer Postal55112
Manufacturer Phone7635052036
Manufacturer G1MEDTRONIC, INC
Manufacturer Street37A CHERRY HILL DR
Manufacturer CityDANVERS MA 01923
Manufacturer CountryUS
Manufacturer Postal Code01923
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameZINGER GUIDE WIRE - CRDM
Generic NameOCCLUDER, CATHETER TIP
Product CodeDQT
Date Received2018-08-27
Returned To Mfg2018-08-09
Model NumberLVZRXT180S
Catalog NumberLVZRXT180S
Lot NumberG15A08517
Device Expiration Date2018-09-20
OperatorHEALTH PROFESSIONAL
Device AvailabilityR
Device AgeDA
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerMEDTRONIC, INC
Manufacturer Address37A CHERRY HILL DR DANVERS MA 01923 US 01923


Patients

Patient NumberTreatmentOutcomeDate
10 2018-08-27

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