VASCU-PICC® MD170126024S (UDI 00884908183139)Recalls & reported problems
Medical Components, Inc. · 2.6F X 50CM DUAL LUMEN VASCU-PICC® W/3F TEARAWAY INTRODUCER SET · Class 2 · Implant
All models of VASCU-PICC (22)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00884908183139), received between Oct 29, 2025 and Mar 6, 2026 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Leak/Splash” (2 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 18, 2026.
Reports received per month
Most reported problems
Device problems
- Leak/Splash2
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.
MalfunctionMar 6, 2026Leak/Splash
PATIENT PICC LINE FOUND TO HAVE A RUPTURED PORTION OF THE LINE AT THE 5CM MARK AND INFILTRATING.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24536492 ↗MalfunctionOct 29, 2025Leak/Splash; Leak/Splash
PATIENT HAD 2.6 FR, DOUBLE LUMEN, MEDCOMP PICC THAT WAS PLACED (B)(6) 2025, THAT WAS FOUND ON (B)(6) 2025 TO BE OUT OF THE INSERTION SITE BY APPROXIMATELY 2 CM. UPON VISUALIZATION OF THE PICC THROUGH THE DRESSING WINDOW, SMALL AREA OF OUTPOUCHING NOTED APPROXIMATELY 0.75 CM FROM HUB. RED LUMEN WAS STILL INFUSING HEPARIN SOLUTION FOR MONITORING OF CVP. WHITE LUMEN WAS FLUSHED PER POLICY, AND SIGNIFICANT LEAKING WAS VISUALIZED AT THE AREA OF OUTPOUCHING THAT WAS PREVIOUSLY MENTIONED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23415495 ↗
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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 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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