ZINGER MEDIUM LVZRMS180S

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2018-07-09 for ZINGER MEDIUM LVZRMS180S manufactured by Medtronic, Inc.

Event Text Entries

[113753321] If information is provided in the future, a supplemental report will be issued.
Patient Sequence No: 1, Text Type: N, H10


[113753322] It was reported that during the implant procedure and placement of the left ventricular (lv) lead, the guidewire was stuck in the lead. The physician chose to replace the lead. No patient complications have been reported as a result of this event.
Patient Sequence No: 1, Text Type: D, B5


[131426405] If information is provided in the future, a supplemental report will be issued.
Patient Sequence No: 1, Text Type: N, H10


MAUDE Entry Details

Report Number1220452-2018-00089
MDR Report Key7671085
Date Received2018-07-09
Date of Report2018-10-03
Date of Event2018-06-13
Date Mfgr Received2018-08-08
Device Manufacturer Date2016-03-28
Date Added to Maude2018-07-09
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 Report0

Device Details

Brand NameZINGER MEDIUM
Generic NameOCCLUDER, CATHETER TIP
Product CodeDQT
Date Received2018-07-09
Returned To Mfg2018-07-09
Model NumberLVZRMS180S
Catalog NumberLVZRMS180S
Lot NumberG16A02433
Device Expiration Date2019-03-28
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 2018-07-09

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