VASCU-PICC® MRVSP26001 (UDI 00884908125108)Recalls & reported problems
Medical Components, Inc. · 2.6F X 50CM DUAL TAPERLESS VASCU-PICC® FULL NURSING KIT W/MAX BARRIER · 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 00884908125108), received between Mar 10, 2017 and Apr 17, 2024 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Break” (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
- Break1
- Leak/Splash1
Patient problems
- Failure of Implant1
- No Clinical Signs, Symptoms or Conditions1
- No Known Impact Or Consequence To Patient1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionApr 17, 2024Leak/Splash; Leak/Splash
RN REPORTED THAT THE WHITE LUMEN ON PICC LINE WAS NONFUNCTIONING AND LEAKING. REPORTED UNABLE TO FLUSH OR ALTEPLASE, WITH DRAINAGE NOTED AROUND THE DRESSING. NEW PICC LINE PLACED, AND OLD NOTE NOTED TO HAVE BREAKAGE ON THE CATHETER.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19123835 ↗MalfunctionMar 10, 2017Break
PATIENT HELD BY FAMILY MEMBERS AND WHILE MOVING AROUND AND BEING HANDLED THE LINE BROKE AT THE CATHETER AND WING CONNECTION. NO HARM TO PATIENT. LINE REMOVED AND REPLACED.
Patient problems: Failure of Implant; No Known Impact Or Consequence To Patient
MAUDE report 6394488 ↗
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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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