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
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
- 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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