ReSolve ConvertX® 00884450458549Recalls & reported problems
Merit Medical Systems, Inc. · Class 2 · Implant
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 2
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00884450458549), received between Dec 8, 2021 and Mar 14, 2023 — classified as 2 injuries.
The most frequently reported specific device problem is “Detachment of Device or Device Component” (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
- Detachment of Device or Device Component1
- Fracture1
- Material Separation1
Patient problems
- No Clinical Signs, Symptoms or Conditions2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
InjuryMar 14, 2023Detachment of Device or Device Component; Detachment of Device or Device Component
THE ACCOUNT ALLEGES THAT DURING THE PROCEDURE THE WIRE BECAME KINKED AND WHEN THE PHYSICIAN TIRED TO CORRECT THE KINK, THE STENT DETACHED. THE PHYSICIAN HAD TO PERFORM A CUT DOWN TO RETRIEVE THE STENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16541651 ↗InjuryDec 8, 2021Fracture; Material Separation; Fracture; Material Separation
THE ACCOUNT ALLEGES THAT DURING A NEPHROURETERAL STENT (NUS) PLACEMENT PROCEDURE, THE CATHETER FRACTURED FOLLOWING THE 3RD AND FINAL STEP OF DEPLOYMENT. RESISTANCE WAS EXPERIENCED BY THE CLINICIAN. THE PATIENT WAS TRANSFERRED TO THE ANGIOGRAPHY SUITE FOR A MORE THOROUGH INVESTIGATION. THE DEVICE WAS SUCCESSFULLY RETRIEVED FROM THE PATIENT AND A NEW STENT WAS SUCCESSFULLY DEPLOYED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 12965422 ↗
Other Stent, ureteral devices
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- Bard® InLay Optima® Ureteral Stent 788626C. R. Bard, Inc. · STENT, URETERAL122 reports
- Bard® InLay® Ureteral Stent with HydroGlide™ Guidewire 777626C. R. Bard, Inc. · STENT, URETERAL118 reports
- Bard® InLay® Ureteral Stent with HydroGlide™ Guidewire 777426C. R. Bard, Inc. · STENT, URETERAL108 reports
- Bard® InLay® Ureteral Stent 778626C. R. Bard, Inc. · STENT, URETERAL100 reports
- Percuflex™ Plus M0061752530Boston Scientific Corporation · STENT, URETERAL1 death99 reports
- Contour VL™ M0061801560Boston Scientific Corporation · STENT, URETERAL1 recall45 reports
- Polaris™ Ultra M0061921330Boston Scientific Corporation · STENT, URETERAL71 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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