Per-Q-Cath Plus Midline Catheter 4143202Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00801741074936), received between Aug 24, 2016 and May 16, 2019 — classified as 2 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 18, 2026.

Most reported problems

Recent adverse event reports

The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

• MalfunctionMay 16, 2019Break; Leak/Splash

  IT WAS REPORTED THAT THE MIDLINE WAS BROKEN/LEAKING. ON (B)(6) 2019: IT WAS REPORTED THAT THE PATIENT WAS PREPPED FOR MIDLINE PLACEMENT, WENT TO PRIME/FLUSH CATHETER IN STERILE KIT, NOTICED LEAKING W/PRIME. NEVER USED, PUT TO SIDE FOR REPORT.

  Patient problems: No Known Impact Or Consequence To Patient

  MAUDE report 8617313 ↗
• MalfunctionAug 24, 2016Break

  PER SALES REPRESENTATIVE, FACILITY CONTACT STATED THAT THE HUB OF A PER-Q-CATH "SNAPPED" OFF WHEN INSIDE THE PATIENT. THE NURSE WAS ABLE TO GRAB THE CATHETER AND THE LINE WAS REMOVED. NO PATIENT INJURY REPORTED. AWAITING ADDITIONAL EVENT DETAILS FROM FACILITY CONTACT INCLUDING IF A NEW CATHETER WAS PLACED. ON (B)(6) 2016 - ADDITIONAL INFORMATION REPORTED BY NURSE STATED THAT A NEW CATHETER WAS PLACED IN THE PATIENT AND THAT THERE WAS NO PATIENT INJURY. NO ADDITIONAL MEDICAL TREATMENT WAS REQUIRED.

  Patient problems: No Known Impact Or Consequence To Patient

  MAUDE report 5901441 ↗