MVP™ MVP-9Q (UDI 00763000307813)Recalls & reported problems
Medtronic, Inc. · PLUG MVP-9Q MICRO VASCULAR · 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 00763000307813), received between Jun 25, 2024 and Jun 25, 2024 — classified as 1 malfunction.
The most frequently reported specific device problem is “Activation, Positioning or Separation Problem” (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.
Reports received per month
Most reported problems
Device problems
- Activation, Positioning or Separation Problem1
- Detachment of Device or Device Component1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionJun 25, 2024Activation, Positioning or Separation Problem; Detachment of Device or Device Component; Activation, Positioning or Separation Problem; Detachment of Device or Device Component
PHYSICIAN ATTEMPTED TO USE A MICROVASCULAR PLUG 9Q DURING PATIENT TREATMENT. THE MVP PLUG WAS SOAKED IN HEPARINIZED SALINE PRIOR TO USE. THE CATHETER WAS FLUSHED BEFORE INSERTING THE PLUG. PHYSICIAN WAS CLOSING A PULMONARY SYSTEMIC COLLATERAL FROM THE INNOMINATE VEIN TO THE LEFT SUPERIOR PULMONARY VEIN. THE COLLATERAL WAS VERY TORTUOUS. NO RESISTANCE WAS FELT WHEN ADVANCING THE PLUG THROUGH THE INTRODUCER SHEATH OR THE CATHETER. PHYSICIAN ADVANCED THE PLUG AND WHEN HE WANTED TO EXPAND THE PLUG, THE EXPANSION WAS SUBOPTIMAL. THE PLUG WAS RE-SHEATHED INTO THE CATHETER FOR REPOSITIONING BUT AT THAT TIME THE PLUG WAS DAMAGED. IT WAS DECIDED TO REMOVE THE PLUG. IT WAS RE-SHEATHED AND AT THAT MOMENT IT WAS CUT, FOR THIS REASON THEY HAD TO REMOVE EVERYTHING AND LOOSE THE POSITION AND DO THE PUNCTURE AGAIN. THE DOCTOR WAS ABLE TO REMOVE THE GUIDE AND PLUG. NO STRUT FRACTURE WAS OBSERVED. A REPLACEMENT PLUG WAS USED WITHOUT ANY PROBLEMS TO COMPLETE THE PROCEDURE. NO MEDICAL OR SURGICAL INTERVENTION WAS NEEDED TO PREVENT A PERMANENT IMPAIRMENT OF A FUNCTION. NO PATIENT SYMPTOMS OR COMPLICATIONS ASSOCIATED WITH THIS EVENT AND DID NOT LEAD TO OR EXTEND PATIENT HOSPITALIZATION. NO PATIENT INJUR
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19608617 ↗
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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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