Curos Jet™ CFJ5-250Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 30707387773831), received between Oct 14, 2019 and Oct 14, 2019 — classified as 1 malfunction.

The most frequently reported specific device problem is “Accessory Incompatible” (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.

• MalfunctionOct 14, 2019Accessory Incompatible; Accessory Incompatible

  A HOSPITAL MATERIALS MANAGER ALLEGED 4-5 INCIDENTS OF FLUID LEAKAGE THAT BEGAN WHEN THEY SWITCHED TO USING BAXTER I.V. CHEMOTHERAPY TUBING IN (B)(6) 2019 AND HAVE BEEN USING CUROS JET¿ DISINFECTING CAP FOR NEEDLELESS CONNECTORS. THE HOSPITAL STAFF PROVIDED INFORMATION REGARDING FOUR ALLEGED INCIDENTS: A WET SPOT WAS FOUND ON THE FLOOR AND THE PORT CLOSEST TO THE PATIENT WAS FOUND TO BE LEAKING, AN I.V. FOUND TO BE LEAKING OUT OF THE PORT WITH THE CUROS JET¿ DISINFECTING CAP ON IT WHERE THE I.V. TUBING WAS CHANGED WITH NO FURTHER LEAKAGE, LEAKAGE AROUND THE CUROS JET¿ DISINFECTING CAP, AND CHEMOTHERAPY LEAKAGE FROM UNDER A PORT UNDERNEATH THE CUROS JET¿ DISINFECTING CAP WHERE THE PRIMARY I.V. LINE HAD NORMAL SALINE INFUSING AND A SECONDARY LINE WAS PIGGY-BACKED INTO A Y-SITE AND INFUSED INTO A PICC LINE, WHERE A NURSE WAS PRESENT AND NOTICED THE LEAKING, STOPPED THE INFUSION RIGHT AWAY, AND ORDERED ANOTHER CHEMOTHERAPY BAG TO INFUSE. PATIENT-SPECIFIC INFORMATION WAS NOT PROVIDED.

  Patient problems: No Known Impact Or Consequence To Patient

  MAUDE report 9185865 ↗