MVP® MVP-3QRecalls & reported problems
Medtronic, Inc. · MVP-3Q MICRO VASCULAR PLUG · Class 2 · Implant
All models of MVP (13)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00847536004344), received between Dec 3, 2019 and Dec 3, 2019 — classified as 1 malfunction.
The most frequently reported specific device problem is “Unintended Ejection” (1 report).
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.
Most reported problems
Device problems
- Unintended Ejection1
Patient problems
- No Known Impact Or Consequence To Patient1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionDec 3, 2019Unintended Ejection; Unintended Ejection
MEDTRONIC RECEIVED REPORT THAT THE MVP UNINTENTIONALLY DETACHED WHEN IT WAS RE-INTRODUCED INTO IS CATHETER OUTSIDE OF THE PATIENT. THE DEVICE WAS NOT ROTATED. THE MVP SYSTEM WAS PREPARED AS INDICATED IN THE INSTRUCTIONS FOR USE (IFU).
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 9407310 ↗
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- Optima Coil System OPTI0413CSFMXBalt USA LLC · Device, Vascular, For Promoting Embolization2 recalls3 reports
- Prestige Coil System PRES0520HPKPLBalt USA LLC · Device, Vascular, For Promoting Embolization2 recalls3 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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