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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: Medtronic Puerto Rico Villalba Attain Ability MRI SureScan; DRUG ELUTING PERMANENT LEFT VENTRICULAR (LV) P

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Medtronic Puerto Rico Villalba Attain Ability MRI SureScan; DRUG ELUTING PERMANENT LEFT VENTRICULAR (LV) P Back to Search Results
Model Number 419688
Medical Device Problem Code Low impedance (2285)
Health Effect - Clinical Code No Clinical Signs, Symptoms or Conditions (4582)
Date of Event 02/22/2026
Type of Reportable Event Malfunction
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Brand Name
Attain Ability MRI SureScan
Common Device Name
DRUG ELUTING PERMANENT LEFT VENTRICULAR (LV) P
Manufacturer (Section D)
Medtronic Puerto Rico Villalba
road 149 km 56.3
villalba PR 00766
Manufacturer (Section G)
Medtronic Puerto Rico Villalba
road 149 km 56.3
villalba PR 00766
Manufacturer Contact
gerard torenvliet
8200 coral sea st ne
mounds view, MN 55112--439
+1(763)526-9277
MDR Report Key50951605
Report Number2649622-2026-28957
Device Sequence Number9624558
Product Code OJX
UDI-Device Identifier00643169860032
UDI-Public(01)00643169860032(17)250125
Combination Product (Y/N)N
Initial Reporter StatePA
Initial Reporter CountryUS
PMA/510(K) Number
P080006
Number of Events Summarized1
Summary Report (Y/N)N
Device Implanted Year2024
Serviced by Third Party (Y/N)N
Reporter Type Manufacturer
Report Source Health Professional
Initial Reporter Occupation Other Health Care Professional
Type of Report Initial
Report Date (Section B) 09/30/2026
1 Device was Involved in the Event
1 Patient was Involved in the Event
Is this an Adverse Event Report? No
Is this a Product Problem Report? Yes
Operator of Device Lay User/Patient
Device Expiration Date01/25/2025
Device Model Number419688
Device Catalogue Number419688
Was Device Available for Evaluation? No
Is the Reporter a Health Professional? Yes
Type of Report(Section G)Thirty-Day
Initial Date Received by Manufacturer 09/08/2026
Initial Report FDA Received Date09/30/2026
Date Device Manufactured02/22/2023
Is the Device Labeled for Single Use? (Y/N) Yes
Is This a Single-Use Device that was
Reprocessed and Reused on a Patient? (Y/N)
No
Patient Sequence Number1
Patient Age83 YR
Patient SexMale
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