PowerPICC Provena CK000951Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00801741202506), received between Jun 1, 2023 and Jun 1, 2023 — classified as 1 malfunction.

The most frequently reported specific device problem is “Defective Component” (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.

• MalfunctionJun 1, 2023Defective Component; Defective Component

  IT WAS REPORTED VIA MEDWATCH, "PATIENT ORDERED TO RECEIVE A DOUBLE LUMEN PICC LINE FOR TPN. THE IV TEAM NURSE WAS SETTING UP THE TRY FOR INSERTION AND PRE-FLUSHING THE CATHETER WAS DONE PRIOR TO STARTING THE PROCEDURE. THE T-PORT THAT WAS ATTACHED TO THE PICC LINE WAS LEAKING FROM THE STOPPER WHEN FLUSHED IN THE LOCATION OF WHERE THE WIRE WAS INSERTED. THE PRODUCT WAS NOT USED FOR INSERTION AND WAS DISPOSED OF. A TRIPLE LUMEN PICC WAS INSERTED INSTEAD WITH DIFFERENT TYPE OF T-PORT ATTACHMENT. NO COMPLICATIONS WERE OBSERVED. NO HARM TO THE PATIENT."

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 17038391 ↗