CT Midline Catheter MLCT5D20Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00884908113754), received between Jan 15, 2020 and Jun 10, 2024 — classified as 2 malfunctions.

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 16, 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.

• MalfunctionJun 10, 2024Break; Break

  DURING MIDLINE POSITIONING MANEUVER IN THE RIGHT BASILICA VEIN, IMPOSSIBILITY OF REMOVING THE METALLIC GUIDE. THE VASCULAR SURGEON IS CONTACTED, WHO REMOVED THE GUIDE WITH THE FINDING OF BRAKING OF IT AND THE PRESENCE OF A FRAGMENT OF THE END, DEEMED TO BE AN EXTRAVASCULAR LEVER, IN THE CONTEXT OF PERIVASCULAR HEMATOMA. ACTIONS: INTERVENTION BY THE VASCULAR SURGEON AND FINDING OF THE BREAKING; METAL GUIDEWIRE REMOVED; ECG RX RIGHT HUMERUS PERFORMED AND VASCULAR RE-ASSESSMENT. NO INDICATION FOR SURGICAL REMOVAL OF THE RETAINED FRAGMENT.

  Patient problems: Hematoma

  MAUDE report 19498076 ↗
• MalfunctionJan 15, 2020Leak/Splash; Leak/Splash

  DURING POWER INFUSION, LEAKAGE IN THE SUBCUTANEOUS TISSUE WAS NOTED. WHEN THE CATHETER WAS REMOVED, A SMALL CRACK WAS NOTED AROUND 2CM FROM THE HUB.

  Patient problems: Hematoma

  MAUDE report 9590526 ↗