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ReSolve® 00884450580714Recalls & reported problems

Merit Medical Systems, Inc. · Class 1

All models of ReSolve (16)

Data updated Oct 16, 2026 from official FDA records · Editorial policy

Adverse event reports
15
Deaths reported
0
Injuries reported
15
Recalls naming it
0

Summary

The FDA's MAUDE database contains 15 adverse event reports that list this exact device (DI 00884450580714), received between Oct 1, 2024 and May 9, 2025 — classified as 15 injuries.

The most frequently reported specific device problem is “Fracture” (15 reports).

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

Nov 2023: 0 reportsDec 2023: 0 reportsJan 2024: 0 reportsFeb 2024: 0 reportsMar 2024: 0 reportsApr 2024: 0 reportsMay 2024: 0 reportsJun 2024: 0 reportsJul 2024: 0 reportsAug 2024: 0 reportsSep 2024: 0 reportsOct 2024: 1 reportsNov 2024: 0 reportsDec 2024: 0 reportsJan 2025: 0 reportsFeb 2025: 0 reportsMar 2025: 0 reportsApr 2025: 0 reportsMay 2025: 14 reportsJun 2025: 0 reportsJul 2025: 0 reportsAug 2025: 0 reportsSep 2025: 0 reportsOct 2025: 0 reportsNov 2025: 0 reportsDec 2025: 0 reportsJan 2026: 0 reportsFeb 2026: 0 reportsMar 2026: 0 reportsApr 2026: 0 reportsMay 2026: 0 reportsJun 2026: 0 reportsJul 2026: 0 reportsAug 2026: 0 reportsSep 2026: 0 reportsOct 2026: 0 reports20242025202614
Last 36 months. The most recent month may be incomplete.

Most reported problems

Device problems

  • Fracture15
  • Material Separation15
  • Material Fragmentation1

Patient problems

  • No Clinical Signs, Symptoms or Conditions15

Recent adverse event reports

The 15 most recent of 15 reports, in the reporter's own words as published by the FDA.

  • InjuryMay 9, 2025Fracture; Material Separation; Fracture; Material Separation

    THE ACCOUNT ALLEGES THAT THE OUTSIDE HUB OF THE RESOLVE LOCKING DRAINAGE CATHETER BROKE/DETACHED AFTER PLACEMENT. THE CATHETERS WERE PLACED FOR ASCITES AND NEPHROSTOMY FLUID DRAINAGE. A NEW DRAINAGE CATHETER WAS PLACED FOR THIS PATIENT. THE DEVICE IS NOT EXPECTED TO RETURN FOR ENGINEERING EVALUATION. ALL DEVICES HAVE BEEN DISCARDED AT THE ACCOUNT.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 21994365 ↗
  • InjuryMay 9, 2025Fracture; Material Separation; Fracture; Material Separation

    THE ACCOUNT ALLEGES THAT THE OUTSIDE HUB OF THE RESOLVE LOCKING DRAINAGE CATHETER BROKE/DETACHED AFTER PLACEMENT. THE CATHETERS WERE PLACED FOR ASCITES AND NEPHROSTOMY FLUID DRAINAGE. A NEW DRAINAGE CATHETER WAS PLACED FOR THIS PATIENT. THE DEVICE IS NOT EXPECTED TO RETURN FOR ENGINEERING EVALUATION. ALL DEVICES HAVE BEEN DISCARDED AT THE ACCOUNT.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 21994357 ↗
  • InjuryMay 9, 2025Fracture; Material Separation; Fracture; Material Separation

    THE ACCOUNT ALLEGES THAT THE OUTSIDE HUB OF THE RESOLVE LOCKING DRAINAGE CATHETER BROKE/DETACHED AFTER PLACEMENT. THE CATHETERS WERE PLACED FOR ASCITES AND NEPHROSTOMY FLUID DRAINAGE. A NEW DRAINAGE CATHETER WAS PLACED FOR THIS PATIENT. THE DEVICE IS NOT EXPECTED TO RETURN FOR ENGINEERING EVALUATION. ALL DEVICES HAVE BEEN DISCARDED AT THE ACCOUNT.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 21994356 ↗
  • InjuryMay 9, 2025Fracture; Material Separation; Fracture; Material Separation

    THE ACCOUNT ALLEGES THAT THE OUTSIDE HUB OF THE RESOLVE LOCKING DRAINAGE CATHETER BROKE/DETACHED AFTER PLACEMENT. THE CATHETERS WERE PLACED FOR ASCITES AND NEPHROSTOMY FLUID DRAINAGE. A NEW DRAINAGE CATHETER WAS PLACED FOR THIS PATIENT. THE DEVICE IS NOT EXPECTED TO RETURN FOR ENGINEERING EVALUATION. ALL DEVICES HAVE BEEN DISCARDED AT THE ACCOUNT.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 21994355 ↗
  • InjuryMay 9, 2025Fracture; Material Separation; Fracture; Material Separation

    THE ACCOUNT ALLEGES THAT THE OUTSIDE HUB OF THE RESOLVE LOCKING DRAINAGE CATHETER BROKE/DETACHED AFTER PLACEMENT. THE CATHETERS WERE PLACED FOR ASCITES AND NEPHROSTOMY FLUID DRAINAGE. A NEW DRAINAGE CATHETER WAS PLACED FOR THIS PATIENT. THE DEVICE IS NOT EXPECTED TO RETURN FOR ENGINEERING EVALUATION. ALL DEVICES HAVE BEEN DISCARDED AT THE ACCOUNT.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 21994354 ↗
  • InjuryMay 9, 2025Fracture; Material Separation; Fracture; Material Separation

    THE ACCOUNT ALLEGES THAT THE OUTSIDE HUB OF THE RESOLVE LOCKING DRAINAGE CATHETER BROKE/DETACHED AFTER PLACEMENT. THE CATHETERS WERE PLACED FOR ASCITES AND NEPHROSTOMY FLUID DRAINAGE. A NEW DRAINAGE CATHETER WAS PLACED FOR THIS PATIENT. THE DEVICE IS NOT EXPECTED TO RETURN FOR ENGINEERING EVALUATION. ALL DEVICES HAVE BEEN DISCARDED AT THE ACCOUNT.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 21994353 ↗
  • InjuryMay 9, 2025Fracture; Material Separation; Fracture; Material Separation

    THE ACCOUNT ALLEGES THAT THE OUTSIDE HUB OF THE RESOLVE LOCKING DRAINAGE CATHETER BROKE/DETACHED AFTER PLACEMENT. THE CATHETERS WERE PLACED FOR ASCITES AND NEPHROSTOMY FLUID DRAINAGE. A NEW DRAINAGE CATHETER WAS PLACED FOR THIS PATIENT. THE DEVICE IS NOT EXPECTED TO RETURN FOR ENGINEERING EVALUATION. ALL DEVICES HAVE BEEN DISCARDED AT THE ACCOUNT.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 21994352 ↗
  • InjuryMay 8, 2025Fracture; Material Separation; Fracture; Material Separation

    THE ACCOUNT ALLEGES THAT THE OUTSIDE HUB OF THE RESOLVE LOCKING DRAINAGE CATHETER BROKE/DETACHED AFTER PLACEMENT. THE CATHETERS WERE PLACED FOR ASCITES AND NEPHROSTOMY FLUID DRAINAGE. A NEW DRAINAGE CATHETER WAS PLACED FOR THIS PATIENT. THE DEVICE IS NOT EXPECTED TO RETURN FOR ENGINEERING EVALUATION. ALL DEVICES HAVE BEEN DISCARDED AT THE ACCOUNT.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 21990162 ↗
  • InjuryMay 8, 2025Fracture; Material Separation; Fracture; Material Separation

    THE ACCOUNT ALLEGES THAT THE OUTSIDE HUB OF THE RESOLVE LOCKING DRAINAGE CATHETER BROKE/DETACHED AFTER PLACEMENT. THE CATHETERS WERE PLACED FOR ASCITES AND NEPHROSTOMY FLUID DRAINAGE. A NEW DRAINAGE CATHETER WAS PLACED FOR THIS PATIENT. THE DEVICE IS NOT EXPECTED TO RETURN FOR ENGINEERING EVALUATION. ALL DEVICES HAVE BEEN DISCARDED AT THE ACCOUNT.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 21990156 ↗
  • InjuryMay 8, 2025Fracture; Material Separation; Fracture; Material Separation

    THE ACCOUNT ALLEGES THAT THE OUTSIDE HUB OF THE RESOLVE LOCKING DRAINAGE CATHETER BROKE/DETACHED AFTER PLACEMENT. THE CATHETERS WERE PLACED FOR ASCITES AND NEPHROSTOMY FLUID DRAINAGE. A NEW DRAINAGE CATHETER WAS PLACED FOR THIS PATIENT. THE DEVICE IS NOT EXPECTED TO RETURN FOR ENGINEERING EVALUATION. ALL DEVICES HAVE BEEN DISCARDED AT THE ACCOUNT.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 21990155 ↗
  • InjuryMay 8, 2025Fracture; Material Separation; Fracture; Material Separation

    THE ACCOUNT ALLEGES THAT THE OUTSIDE HUB OF THE RESOLVE LOCKING DRAINAGE CATHETER BROKE/DETACHED AFTER PLACEMENT. THE CATHETERS WERE PLACED FOR ASCITES AND NEPHROSTOMY FLUID DRAINAGE. A NEW DRAINAGE CATHETER WAS PLACED FOR THIS PATIENT. THE DEVICE IS NOT EXPECTED TO RETURN FOR ENGINEERING EVALUATION. ALL DEVICES HAVE BEEN DISCARDED AT THE ACCOUNT.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 21990154 ↗
  • InjuryMay 8, 2025Fracture; Material Separation; Fracture; Material Separation

    THE ACCOUNT ALLEGES THAT THE OUTSIDE HUB OF THE RESOLVE LOCKING DRAINAGE CATHETER BROKE/DETACHED AFTER PLACEMENT. THE CATHETERS WERE PLACED FOR ASCITES AND NEPHROSTOMY FLUID DRAINAGE. A NEW DRAINAGE CATHETER WAS PLACED FOR THIS PATIENT. THE DEVICE IS EXPECTED TO RETURN FOR A FULL ENGINEERING EVALUATION.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 21990152 ↗
  • InjuryMay 8, 2025Fracture; Material Separation; Fracture; Material Separation

    THE ACCOUNT ALLEGES THAT THE OUTSIDE HUB OF THE RESOLVE LOCKING DRAINAGE CATHETER BROKE/DETACHED AFTER PLACEMENT. THE CATHETERS WERE PLACED FOR ASCITES AND NEPHROSTOMY FLUID DRAINAGE. A NEW DRAINAGE CATHETER WAS PLACED FOR THIS PATIENT. THE DEVICE IS EXPECTED TO RETURN FOR A FULL ENGINEERING EVALUATION.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 21990150 ↗
  • InjuryMay 8, 2025Fracture; Material Separation; Fracture; Material Separation

    THE ACCOUNT ALLEGES THAT THE OUTSIDE HUB OF THE RESOLVE LOCKING DRAINAGE CATHETER BROKE/DETACHED AFTER PLACEMENT. THE CATHETERS WERE PLACED FOR ASCITES AND NEPHROSTOMY FLUID DRAINAGE. A NEW DRAINAGE CATHETER WAS PLACED FOR THIS PATIENT. THE DEVICE IS NOT EXPECTED TO RETURN FOR ENGINEERING EVALUATION. ALL DEVICES HAVE BEEN DISCARDED AT THE ACCOUNT.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 21990141 ↗
  • InjuryOct 1, 2024Fracture; Material Fragmentation; Material Separation; Fracture; Material Fragmentation; Material Separation

    THE ACCOUNT ALLEGES THAT DURING THE SMALL BOWEL ANASTOMOSIS DRAINAGE CATHETER REMOVAL, THE DRAINAGE CATHETER FRACTURED INTO THREE PIECES. THE FOREIGN BODIES WERE SUCCESSFULLY REMOVED VIA A VASCULAR SNARE DEVICE. AS A RESULT OF THIS EVENT, A PROLONGATION OF HOSPITALIZATION WAS REQUIRED FOR THIS PATIENT. THE PHYSICIAN DOES NOT BELIEVE THAT EXCESSIVE FORCE WAS USED DURING DEVICE REMOVAL. THE PATIENT TOLERATED THE PROCEDURE WELL. NO ADDITIONAL PATIENT CONSEQUENCES TO REPORT.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 20349151 ↗

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Sources and updates

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