• Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

MAUDE Adverse Event Report: MEDTRONIC IRELAND MICRA; LEADLESS PACEMAKER

  • Print
  • Share
  • E-mail
-
Super Search Devices@FDA
510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
CFR Title 21 | Radiation-Emitting Products | X-Ray Assembler | Medsun Reports | CLIA | TPLC
 

MEDTRONIC IRELAND MICRA; LEADLESS PACEMAKER Back to Search Results
Model Number MC1VR01US
Device Problems Battery Problem (2885); High Capture Threshold (3266)
Patient Problem No Known Impact Or Consequence To Patient (2692)
Event Date 07/09/2019
Event Type  malfunction  
Manufacturer Narrative
If information is provided in the future, a supplemental report will be issued.
 
Event Description
It was reported that the leadless implantable pulse generator (ipg) exhibited high thresholds.It was also reported that the ipg shows only eight to ten months remaining on battery.The ipg remains in use.No patient complications have been reported as a result of this event.
 
Search Alerts/Recalls

  New Search  |  Submit an Adverse Event Report

Brand Name
MICRA
Type of Device
LEADLESS PACEMAKER
Manufacturer (Section D)
MEDTRONIC IRELAND
parkmore business park west
galway
Manufacturer (Section G)
MEDTRONIC IRELAND
parkmore business park west
galway
Manufacturer Contact
paula bixby
8200 coral sea st ne
mounds view, MN 55112
7635055378
MDR Report Key8850365
MDR Text Key152953263
Report Number9612164-2019-03179
Device Sequence Number1
Product Code PNJ
UDI-Device Identifier00643169711761
UDI-Public00643169711761
Combination Product (y/n)N
Reporter Country CodeUS
PMA/PMN Number
P150033
Number of Events Reported1
Summary Report (Y/N)N
Report Source Manufacturer
Source Type company representative
Reporter Occupation Non-Healthcare Professional
Type of Report Initial
Report Date 08/01/2019
1 Device was Involved in the Event
1 Patient was Involved in the Event
Date FDA Received08/01/2019
Is this a Product Problem Report? Yes
Device Operator Lay User/Patient
Device Expiration Date07/14/2020
Device Model NumberMC1VR01US
Device Catalogue NumberMC1VR01US
Was Device Available for Evaluation? No
Date Manufacturer Received07/09/2019
Date Device Manufactured02/07/2019
Is the Device Single Use? Yes
Is This a Reprocessed and Reused Single-Use Device? No
Type of Device Usage Initial
Patient Sequence Number1
Patient Age83 YR
-
-