Poly Per-Q-Cath Catheter 3153108Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00801741034817), received between Jun 1, 2016 and Jun 1, 2016 — 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.

• InjuryJun 1, 2016Break

  ON 5/11/16 - IT WAS REPORTED BY THE COMPLAINANT THAT DURING SURGERY OVER THE WEEKEND, A PICC WAS USED ON A PATIENT. WHEN THE STYLET WAS REMOVED FROM THE PATIENT IT WAS NOTED THAT A FRAGMENT OF THE STYLET WAS BROKEN OFF 20 CENTIMETERS FROM THE DISTAL END. PATIENT HAD TO BE SENT TO ANOTHER FACILITY FOR RETRIEVAL OF THE BROKEN PIECE. ON 5/12/16 - RECEIVED AN EMAIL WITH ADDITIONAL INFORMATION REGARDING THE EVENT. CONTACT REPORTED THAT THE FRAGMENT OF THE STYLET WAS REMOVED SUCCESSFULLY. NO HARM TO THE PATIENT WAS REPORTED.

  Patient problems: No Known Impact Or Consequence To Patient

  MAUDE report 5691338 ↗