Smart Port CT H787CT66PTPD0Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 15051684017985), received between May 20, 2025 and Jun 11, 2026 — classified as 2 injuries.

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.

• InjuryJun 11, 2026Adverse Event Without Identified Device or Use Problem

  ON OR ABOUT ON (B)(6) 2013, PLAINTIFF UNDERWENT PLACEMENT OF AN ANGIODYNAMICS SMARTPORT CT PORT CATHETER PRODUCT, WITH MODEL NUMBER: CT66PTPD, AND LOT NUMBER: 602766. THIS SMARTPORT DEVICES CONSISTED OF A PORT BODY AND A POLYURETHANE CATHETER. THE SMARTPORT DEVICE WAS IMPLANTED VIA THE RIGHT INTERNAL JUGULAR VEIN BY DR. (B)(6), M.D., AT THE (B)(6), FOR THE PURPOSE OF ONGOING CHEMOTHERAPY TREATMENT. ON OR ABOUT ON (B)(6) 2014, PLAINTIFF PRESENTED TO THE (B)(6) IN (B)(6), WITH COMPLAINTS OF A MALFUNCTIONING PORT. A VENOUS ULTRASOUND WAS PERFORMED FOR EVALUATION OF A POTENTIAL THROMBOSIS. THE ULTRASOUND IDENTIFIED A NEAR OCCLUSIVE THROMBUS WITHIN THE INTERNAL JUGULAR VEIN AND PROXIMAL SUBCLAVIAN VEIN, WHICH REQUIRED THE PORT TO BE REMOVED. DUE TO THE ONGOING NEED FOR VENOUS ACCESS, A DECISION WAS MADE BY PLAINTIFF'S PHYSICIANS TO LEAVE THE PORT IN PLACE UNTIL TREATMENT WAS COMPLETED. ON OR ABOUT ON (B)(6) 2014, PLAINTIFF UNDERWENT REMOVAL OF THE SMARTPORT. THE PROCEDURE WAS PERFORMED BY DR. (B)(6), M.D., AT THE (B)(6) IN (B)(6).

  Patient problems: Thrombosis/Thrombus

  MAUDE report 25480892 ↗
• InjuryMay 20, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  ON OR ABOUT (B)(6) 2021, PLAINTIFF UNDERWENT PLACEMENT OF THE FOLLOWING ANGIODYNAMICS' SMARTPORT CT PRODUCT: MODEL/CAT NUMBER: H787CT66PTPD0, LOT NUMBER: 5692897, FOR THE PURPOSES OF PLAINTIFF'S CHEMOTHERAPY. UPON INFORMATION AND BELIEF, THE AFOREMENTIONED DEVICE'S DESCRIPTION IS AS FOLLOWS: SMART PORT CT PERIPHERAL/CHEST TITANIUM PORT SYSTEM WITH ATTACHABLE 6.6F X 55CM POLYURETHANE CATHETER AND 7F INTRODUCER KIT. ON OR ABOUT (B)(6) 2021, THE DEVICE AT ISSUE WAS IMPLANTED BY DR. (B)(6), AT (B)(6), FOR THE PURPOSES INDICATED ABOVE. UPON INFORMATION AND BELIEF, ON (B)(6) 2022, PLAINTIFF PRESENTED TO (B)(6) HOSPITAL, WHERE PLAINTIFF WAS THEN DIAGNOSED WITH BACTEREMIA AND SHORTNESS OF BREATH. UPON INFORMATION AND BELIEF, ON OR ABOUT (B)(6) 2022, PLAINTIFF WAS ALSO DIAGNOSED WITH ACUTE EMBOLISM AND THROMBOSIS OF SUPERFICIAL VEINS OF RIGHT UPPER EXTREMITY. ON OR ABOUT (B)(6) 2022, PLAINTIFF'S BACTEREMIA WAS NOTED TO BE MRSA BACTEREMIA BY (B)(6), MD, ATTENDING PHYSICIAN, (B)(6) MEDICAL CENTER. DR. (B)(6) NOTED THAT PLAINTIFF'S MRSA BACTEREMIA'S LIKELY SOURCE WAS PLAINTIFF'S PORT. ON OR ABOUT (B)(6) 2022, PLAINTIFF'S BLOOD, BACTERIOLOGY CULTURE'S 1ST SET'S RESULTS SHOWED THE GROWTH OF STAP

  Patient problems: Bacteremia; Dyspnea; Embolism/Embolus; Thrombosis/Thrombus

  MAUDE report 22057459 ↗