PowerPICC SOLO CK000361Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00801741087509), received between Jan 10, 2019 and Jan 10, 2019 — classified as 1 malfunction.

The most frequently reported specific device problem is “Material Frayed” (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 16, 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.

• MalfunctionJan 10, 2019Material Frayed; Physical Resistance/Sticking

  IT WAS REPORTED THAT "DURING PICC PLACEMENT ENCOUNTERED PROBLEM WITH MST WIRE. VESSEL ACCESSED WITH NEEDLE, UNABLE TO THREAD WIRE, RE-POSITIONED NEEDLE ATTEMPTED TO THREAD WIRE MET RESISTANCE AGAIN. WIRE ESTIMATED TO BE JUST PAST THE TIP OF THE NEEDLE. I ATTEMPTED TO PULL WIRE OUT, MET RESISTANCE IN PULLING WIRE OUT. I HAD TO PULL THE NEEDLE AND WIRE OUT AS A UNIT. THE WIRE HAD FRAYED AND I HAD TO PULL LONG STRING LIKE WIRE THE REMAINING WAY OUT OF THE PATIENTS ARM. NEW MST KIT USED AND VEIN WAS ACCESSED WITHOUT PROBLEMS."

  Patient problems: No Known Impact Or Consequence To Patient

  MAUDE report 8235787 ↗