ReSolve® 00884450230244Recalls & 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
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00884450230244), received between May 21, 2024 and May 21, 2024 — classified as 1 injury.
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
- Adverse Event Without Identified Device or Use Problem1
Patient problems
- Skin Infection1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryMay 21, 2024Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
REVIEW OF PMCF SURVEY DATA FOR THE RESOLVE PRODUCT FAMILY IDENTIFIED AN INCIDENT INVOLVING AN RESOLVE NON-LOCKING DRAINAGE CATHETER. THE ACCOUNT ALLEGES WHILE TREATING A FEMALE PATIENT, WITH CONGESTIVE HEART FAILURE, THE CATHETER WAS USED FOR PERCUTANEOUS DRAINAGE OF NON-BILIARY FLUIDS IN THE ABDOMEN. THE DEVICE WAS IMPLANTED FOR 3 DAYS AND DURING THIS TIME THE PATIENT EXPERIENCED A SKIN INFECTION. ADDITIONAL TREATMENT WAS NECESSARY. NO ADDITIONAL PATIENT CONSEQUENCE TO REPORT.
Patient problems: Skin Infection
MAUDE report 19361621 ↗
Other CATHETER, IRRIGATION devices
- Navarre Opti-Drain NOD8LPTBard Access Systems, Inc. · CATHETER, IRRIGATION901 reports
- Navarre NNU8LPTBard Access Systems, Inc. · CATHETER, IRRIGATION736 reports
- BLAKE 2227Ethicon Inc. · CATHETER, IRRIGATION331 reports
- Navarre NNU6LPTBard Access Systems, Inc. · CATHETER, IRRIGATION211 reports
- Navarre Opti-Drain NOD10LPTBard Access Systems, Inc. · CATHETER, IRRIGATION178 reports
- Navarre NNU10LPTBard Access Systems, Inc. · CATHETER, IRRIGATION127 reports
- BLAKE 2233Ethicon Inc. · CATHETER, IRRIGATION114 reports
- Vasoshield VH-5001Maquet Cardiovascular LLC · Catheter, Irrigation1 recall27 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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