Total Abscession 14000823Recalls & reported problems
Angiodynamics, Inc. · 8F x 30cm Total Abscession General Drainage Catheter (Locking Pigtail) · Class 1
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI H787140008230), received between Mar 18, 2025 and Mar 18, 2025 — classified as 1 malfunction.
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 18, 2026.
Reports received per month
Most reported problems
Device problems
- Detachment of Device or Device Component1
Patient problems
- Device Embedded In Tissue or Plaque1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionMar 18, 2025Detachment of Device or Device Component; Detachment of Device or Device Component
AN END USER REPORTED AN ISSUE WITH A TOTAL ABSCESSION DRAINAGE CATHETER GEN 8F X 30CM WITHOUT R/O BAND.THE CATHETER WAS USED DURING A CT-GUIDED CYST DRAINAGE AND SCLEROTHERAPY. WHEN THE CATHETER WAS BEING REMOVED FROM PATIENT, THE TECH NOTED THAT THE TIP OF THE CATHETER WAS MISSING. A CT OF PELVIS CONFIRMED PRESENCE OF RETAINED TIP IN THE ENDOMETRIOMA. THERE WAS AN ATTEMPT TO REMOVE THE TIP WITH A PERCUTANEOUS PROCEDURE, BUT WAS UNSUCCESSFUL DUE TO IT BEING EMBEDDED IN THE TISSUE.
Patient problems: Device Embedded In Tissue or Plaque
MAUDE report 21631464 ↗
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 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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