Curos Jet™ CFJ1-270Recalls & reported problems

Summary

The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 30707387773824), received between Apr 30, 2019 and Nov 17, 2019 — classified as 1 injury, 2 malfunctions.

The most frequently reported specific device problem is “Accessory Incompatible” (3 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 3 most recent of 3 reports, in the reporter's own words as published by the FDA.

• MalfunctionNov 17, 2019Accessory Incompatible; Accessory Incompatible

  A DISTRIBUTOR REPORTED THAT A PATIENT HAD DOBUTAMINE INFUSING THROUGH AN INTERNAL JUGULAR CATHETER WITH PARTIAL OCCLUSION AND HAD LEAKING AT THE CUROS JET¿ DISINFECTING CAPS Y-SITE. NO PATIENT HARM OCCURRED. NO ADDITIONAL INFORMATION WAS PROVIDED.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 9333361 ↗
• MalfunctionOct 29, 2019Accessory Incompatible; Accessory Incompatible

  A CLINICAL NURSE SPECIALIST IN HEMATOLOGY-ONCOLOGY ALLEGED THAT A POOL OF LIQUID WAS FOUND UNDER A PATIENT'S BED WHEN A PATIENT HAD CHEMOTHERAPY (CYTOXAN) INFUSING (200ML BAG OVER 2 HOURS) THAT WAS PIGGY BACKED INTO A Y-SITE OF THE PRIMARY TUBING OF A TRIPLE LUMEN HICKMAN CATHETER. THE Y-SITE, CLOSEST TO THE PATIENT, WHICH HAD A CUROS JET¿ DISINFECTING CAP FOR NEEDLELESS CONNECTORS ON IT REPORTEDLY LEAKED. THE MEDICATION WAS RE-DOSED FOR THE PATIENT.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 9252231 ↗
• InjuryApr 30, 2019Accessory Incompatible; Accessory Incompatible

  A NURSE REPORTED 3M¿ CUROS JET¿ DISINFECTING CAPS WERE PLACED ON THE NEEDLELESS CONNECTOR PORTS OF A PATIENT'S IV TUBING. THE NURSE REPORTED A CUROS CAP "FAILED" ON ONE OF THE NEEDLELESS CONNECTOR PORTS AND A PUDDLE OF PROPOFOL IV MEDICATION WAS FOUND ON THE FLOOR UNDERNEATH THE IV PORT. THE NURSE REPORTED THIS RESULTED IN THE PATIENT NOT RECEIVING THE APPROPRIATE DOSE OF MEDICATION. NO ADDITIONAL INFORMATION HAS BEEN RECEIVED TO DATE.

  Patient problems: Underdose

  MAUDE report 8565291 ↗