Hohn Catheter for Central Venous Placement 0600710Recalls & reported problems

Summary

The FDA's MAUDE database contains 6 adverse event reports that list this exact device (DI 00801741036361), received between Oct 26, 2016 and Oct 23, 2019 — classified as 6 malfunctions.

The most frequently reported specific device problem is “Fluid/Blood Leak” (6 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 6 most recent of 6 reports, in the reporter's own words as published by the FDA.

• MalfunctionOct 23, 2019Fluid/Blood Leak; Fluid/Blood Leak

  IT WAS REPORTED VIA MEDWATCH, "ATTEMPTED TO FLUSH PATIENT'S RED LUMEN OF RIGHT INTERNAL JUGULAR HOHN CATHETER AND THE LINE PERFORATED. THE CLAMP WAS MOVED CLOSER TO THE PATIENT AND THE LUMEN WAS DE-ACCESSED AND REPLACED IN INTERVENTIONAL RADIOLOGY."

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 9224652 ↗
• MalfunctionOct 23, 2019Fluid/Blood Leak; Fluid/Blood Leak

  IT WAS REPORTED VIA MEDWATCH, "A HOLE WAS NOTED IN THE HOHN CATHETER. THE PATIENT WAS SENT TO IR FOR AN EXCHANGER."

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 9224651 ↗
• MalfunctionOct 22, 2019Fluid/Blood Leak; Fluid/Blood Leak

  IT WAS REPORTED VIA MEDWATCH, "ONE LUMEN ON THE DOUBLE LUMEN HOHN CATHETER WAS NOT EASY TO FLUSH. WHEN FLUSHED, A HOLE WAS FOUND IN THE TUBING OF THE HOHN CATHETER. TEAM WAS NOTIFIED AND LUMEN WAS CLAMPED CLOSER TO THE SKIN. THE HOHN CATHETER WAS REPLACED BY IR."

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 9221266 ↗
• MalfunctionOct 22, 2019Fluid/Blood Leak; Fluid/Blood Leak

  IT WAS REPORTED VIA MEDWATCH, "A HOLE WAS IDENTIFIED IN THE HOHN CATHETER. THE PATIENT WAS SENT TO IR TO HAVE THE HOHN CATHETER EXCHANGED." NO OTHER INFORMATION PROVIDED.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 9219860 ↗
• MalfunctionOct 15, 2019Fluid/Blood Leak; Fluid/Blood Leak

  IT WAS REPORTED VIA MEDWATCH, "DURING AN INFUSION THE BARD CVC WAS LEAKING. THE LINE WAS EXCHANGED IN INTERVENTIONAL RADIOLOGY."

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 9194219 ↗
• MalfunctionOct 26, 2016Fluid/Blood Leak

  HEALTH PROFESSIONAL REPORTED THAT A HOHN CATHETER WAS INSERTED IN A PATIENT ON (B)(6) 2016 AND IT WAS USED ON TWO OCCASIONS. IT WAS CONNECTED TO A PUMP WHICH THE PATIENT WENT HOME WITH. THE PATIENT CAME TO HOSPITAL FOR INFUSION AND FOLLOW UP ON (B)(6) 2016. AFTER INFUSION, WHEN THE NURSE FLUSHED THE CATHETER, IT WAS FOUND THAT THE GAUZE WAS WET AND PATIENT COMPLAINED OF PAIN. PATIENT WAS SENT TO THE IR AND IT WAS FOUND THAT THE CATHETER WAS LEAKING AT THE INSERTION SITE. THE CATHETER WAS TAKEN OUT OF THE PATIENT AND A NEW HOHN CATHETER WAS INSERTED.

  Patient problems: Pain

  MAUDE report 6057941 ↗