Smart Port CT H787CT66PTPDVI1Recalls & reported problems
Angiodynamics, Inc. · Smart Port CT Peripheral/Chest Titanium Port System with Attachable 6.6F x 55cm Polyurethane Catheter and 7F Introducer Kit (with Valved Introducer) · Class 2 · Implant
All models of Smart Port CT (36)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 15051684018111), received between Sep 18, 2025 and Sep 18, 2025 — classified as 1 injury.
The most frequently reported specific device problem is “Migration” (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.
Reports received per month
Most reported problems
Device problems
- Migration1
- Obstruction of Flow1
Patient problems
- Obstruction/Occlusion1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjurySep 18, 2025Obstruction of Flow; Migration; Obstruction of Flow; Migration
ON OR ABOUT ON (B)(6) 2022, DECEDENT PLAINTIFF UNDERWENT PLACEMENT OF AN ANGIODYNAMICS SMARTPORT PRODUCT, REFERENCE NUMBER: (B)(4), LOT NUMBER: 5760651. THE DEVICE WAS IMPLANTED BY DR. (B)(6), MD, AT (B)(6), FOR THE PURPOSE OF ADMINISTERING CHEMOTHERAPY. ON OR ABOUT ON (B)(6) 2023, DECEDENT PLAINTIFF'S SMARTPORT WOULD NOT ASPIRATE. AS A RESULT OF THE FAILURE TO ASPIRATE, THE SMARTPORT WAS CHECKED AND DEMONSTRATED THAT THE CATHETER TIP RESIDED IN THE AZYGOUS VEIN. SINCE THE CATHETER TIP DEMONSTRATED MIGRATION FROM ITS ORIGINAL RIGHT ATRIUM PLACEMENT, PORT REVISION/REPOSITIONING WAS RECOMMENDED. ON OR ABOUT ON (B)(6) 2023, A FOLLOW-UP SVC VENOGRAPHY DEMONSTRATED COMPLETE SVC OCCLUSION AND AN ULTRASOUND OF THE RIGHT INTRAJUGULAR VEIN DEMONSTRATED OCCLUSION AS WELL. AS A RESULT OF THESE FINDINGS, DOCTORS RECOMMENDED HAVING THE SMARTPORT REMOVED. ON OR ABOUT ON (B)(6) 2023, DECEDENT PLAINTIFF'S DEFECTIVE PORT WAS REMOVED BY DR. (B)(6), MD AT (B)(6) HOSPITAL. DECEDENT PLAINTIFF SUFFERED SUFFER PHYSICAL PAIN AND MENTAL ANGUISH, WHICH LASTED UNTIL HIS DEATH ON (B)(6) 2024.
Patient problems: Obstruction/Occlusion
MAUDE report 23088381 ↗
Other PORT & CATHETER, IMPLANTED, SUBCUTANEOUS, INTRAVASCULAR devices
- PowerPort M.R.I., Groshong 9808560Bard Access Systems, Inc. · PORT & CATHETER, IMPLANTED, SUBCUTANEOUS, INTRAVASCULAR3 deaths834 reports
- PowerPort ClearVUE 1608062Bard Access Systems, Inc. · PORT & CATHETER, IMPLANTED, SUBCUTANEOUS, INTRAVASCULAR18 deaths571 reports
- PowerPort ClearVUE 5608062Bard Access Systems, Inc. · PORT & CATHETER, IMPLANTED, SUBCUTANEOUS, INTRAVASCULAR31 deaths542 reports
- PowerPort M.R.I., ChronoFlex 1808000Bard Access Systems, Inc. · PORT & CATHETER, IMPLANTED, SUBCUTANEOUS, INTRAVASCULAR19 deaths513 reports
- PowerPort M.R.I., ChronoFlex 1808060Bard Access Systems, Inc. · PORT & CATHETER, IMPLANTED, SUBCUTANEOUS, INTRAVASCULAR1 recall15 deaths383 reports
- PowerPort M.R.I., Groshong 1808560Bard Access Systems, Inc. · PORT & CATHETER, IMPLANTED, SUBCUTANEOUS, INTRAVASCULAR10 deaths304 reports
- PowerPort M.R.I., ChronoFlex 1829500Bard Access Systems, Inc. · PORT & CATHETER, IMPLANTED, SUBCUTANEOUS, INTRAVASCULAR6 deaths197 reports
- BardPort M.R.I. 0602680Bard Access Systems, Inc. · PORT & CATHETER, IMPLANTED, SUBCUTANEOUS, INTRAVASCULAR2 deaths179 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
How reports and recalls are matched · Editorial policy · Report an error on this page