First PICC™ 384242Recalls & reported problems
Argon Medical Devices, Inc. · First PICC™ S/L Peripherally Inserted Central Catheter 26ga (1.9F) 0.65mm x 50cm with Statlock® Stabilization Device · Class 2 · Implant
Data updated Oct 16, 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 00886333209774), received between May 10, 2023 and Apr 26, 2024 — classified as 3 malfunctions.
The most frequently reported specific device problem is “Break” (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 16, 2026.
Reports received per month
Most reported problems
Device problems
- Break2
- Material Split, Cut or Torn1
Patient problems
- Insufficient Information3
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
MalfunctionApr 26, 2024Break; Break
REPORTER INDICATED THEY PLACED A1.9 FR SINGLE LUMEN PICC ON NEONATE FOR THE INPATIENT PEDS FLOOR AND HAS BROKEN JUST PRIOR TO THE DISC UNDER THE TEGADERM USING THE STATLOCK ON (B)(6) 2024.
Patient problems: Insufficient Information
MAUDE report 19189251 ↗MalfunctionApr 26, 2024Break; Break
THE REPORTER INDICATED THEY PLACED A SINGLE LUMEN PICC ON NEONATES ON (B)(6) 2023 FOR THE INPATIENT PEDS FLOOR AND HAS BROKEN JUST PRIOR TO THE DISC UNDER THE TEGADERM USING THE STATLOCK.
Patient problems: Insufficient Information
MAUDE report 19189225 ↗MalfunctionMay 10, 2023Material Split, Cut or Torn; Material Split, Cut or Torn
FOUND THAT THE IV FLUIDS WERE "LEAKING" UPON FURTHER INVESTIGATION THEY FOUND THAT THE CLEAR "TAIL" BETWEEN THE HUB AND THE IV CONNECTION (THE ONE WITH THE WRITING ON IT) HAD SPLIT VERTICALLY.
Patient problems: Insufficient Information
MAUDE report 16903378 ↗
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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 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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