VASCU-PICC® MD17022601 (UDI 00884908146462)Recalls & reported problems
Medical Components, Inc. · 2.6F X 50CM DUAL LUMEN2.6F X 50C VASCU-PICC®WITHOUT OTN · Class 2 · Implant
All models of VASCU-PICC (22)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 3
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 00884908146462), received between May 3, 2023 and May 3, 2023 — classified as 3 malfunctions.
The most frequently reported specific device problem is “Leak/Splash” (3 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.
Most reported problems
Device problems
- Leak/Splash3
Patient problems
- Swelling/ Edema2
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
MalfunctionMay 3, 2023Leak/Splash; Leak/Splash
PICC REMOVAL CHARTED AS LEAKING AT SITE, CATHETER CRACKED. PATIENT ARM WITH EDEMA.
Patient problems: Swelling/ Edema
MAUDE report 16860518 ↗MalfunctionMay 3, 2023Leak/Splash; Leak/Splash
CATHETER NOTED TO BE LEAKING AT SITE. PICC LINE EXCHANGED WITHOUT COMPLICATION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16860468 ↗MalfunctionMay 3, 2023Leak/Splash; Leak/Splash
EDEMA NOTED TO PATIENT'S ARM. LEAKING PRESENT AT INSERTION SITE. PICC LINE REMOVED AND NOTED TO HAVE A TEAR AT THE 1 CM MARK.
Patient problems: Swelling/ Edema
MAUDE report 16860354 ↗
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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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