Poly RadPICC Catheter 3165135Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00801741034954), received between Apr 4, 2018 and Apr 4, 2018 — classified as 1 injury.

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.

Most reported problems

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

• InjuryApr 4, 2018Break

  IT WAS REPORTED THAT THE TIP OF THE PICC BROKE OFF IN THE PATIENT DURING INSERTION WHILE THE PATIENT WAS AN INPATIENT. THE HEALTH CARE PROFESSIONAL ASSISTING THE PHYSICIAN WITH THE PROCEDURE REPORTED THAT A PIECE F THE GUIDEWIRE BROKE OFF IN THE PATIENT'S LEFT ARM AND WAS NOT RETRIEVED AND THE DEVICE WAS NOT PLACED. THEY ALSO STATE THAT PATIENT WAS NOTIFIED. IT WAS REPORTED THAT THE PATIENT CAME BACK TO THE FACILITY FOR X-RAYS/ULTRASOUND ON (B)(6) 2017 AND THE DEVICE WAS NOT RETRIEVED.

  Patient problems: No Known Impact Or Consequence To Patient

  MAUDE report 7396158 ↗