MVP™ MVP-7Q (UDI 00763000307806)Recalls & reported problems

Summary

The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 00763000307806), received between Nov 14, 2023 and Apr 8, 2025 — classified as 1 injury, 2 malfunctions.

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.

Most reported problems

Recent adverse event reports

The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.

• MalfunctionApr 8, 2025Use of Device Problem; Use of Device Problem

  IT WAS REPORTED WITH LIMITED INFORMATION THAT A MICRO VASCULAR PLUG WAS USED PAST ITS USE BY DATE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 21796644 ↗
• MalfunctionMar 13, 2024Detachment of Device or Device Component; Detachment of Device or Device Component

  PHYSICIAN WAS ATTEMPTING TO USE A MICROVASCULAR PLUG 7Q DURING PROCEDURE. IT WAS REPORTED THE MICROVASCULAR PLUG RELEASED ON ITS OWN, WITHOUT ANTI TORQUE RELEASE SYSTEM. MVP PLUG WAS SOAKED IN HEPARINIZED SALINE PRIOR TO USE. A 5FR CATHETER WAS USED. CATHETER WAS FLUSHED BEFORE INSERTING THE PLUG AND A CONTINUOUS FLUSH WAS MAINTAINED DURING THE PROCEDURE. THERE WAS NO BREAK OR KINK ON THE PLUG NOTED. NO RESISTANCE WAS FELT WHEN ADVANCING THE PLUG THROUGH THE INTRODUCER SHEATH OR CATHETER. IT WAS REPORTED THAT PREMATURE DEPLOYMENT OCCURRED INSIDE THE PATIENT. NO DEFORMATION WAS NOTED TO THE DEPLOYED PLUG. THE DELIVERY SYSTEM WAS REMOVED FROM PATIENT AND THE PLUG REMAINED IN THE PATIENT WITH NO VESSEL DAMAGED. NO PATIENT INJURY REPORTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 18895779 ↗
• InjuryNov 14, 2023Difficult to Remove; Activation, Positioning or Separation Problem; Difficult to Remove; Activation, Positioning or Separation Problem

  AN MVP WAS INTENDED TO BE USED. IT WAS REPORTED THE PRODUCT COULD NOT BE RELEASED IN THE VESSEL. THE PLUG COULD NOT BE REMOVED VIA THE SCREW THREAD IN THE VESSEL. SINCE THE PLUG WAS ALREADY OPENED IN THE VESSEL AND COULD NO LONGER BE FOLDED OVER THE NORMAL CATHETER, THE PLUG HAD TO BE RETRIEVED USING A SHEATH RETRACTION VIA THE SHEATH. THE WITHDRAWAL COULD BE CARRIED OUT WITHOUT ANY VASCULAR DAMAGE TO THE PATIENT. NO SERIOUS CONSEQUENCES FOR THE PATIENT, USER OR THIRD PARTY. THE INTERVENTION WAS DELAYED FOR A MOMENT BECAUSE THE PLUG HAD TO BE RECOVERED AND A NEW SYSTEM HAD TO BE PREPARED. THERE IS A POTENTIAL RISK THAT THE OPENED PLUG COULD INJURE A VESSEL WHEN WITHDRAWN. NO PATIENT INJURY.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 18135887 ↗