Home › Device types › LJT
Port & Catheter, Implanted, Subcutaneous, Intravascular
FDA product code LJT · Class 2 · General Hospital
1,557
Registered devices
22,887
Adverse events
141
Recalls
288
510(k) clearances
Devices with this code
Vital-Port — COOK INCORPORATEDBioFlo Vortex — Angiodynamics, Inc.BioFlo — Angiodynamics, Inc.PowerPort M.R.I. — Bard Access Systems, Inc.Dignity® Mid-Sized CT Port — Medical Components, Inc.PowerPort, ChronoFlex — Bard Access Systems, Inc.Pro-Fuse® Low Profile CT Port — Medical Components, Inc.Xcela — NAVILYST MEDICAL, INC.Jet Port Plus II — PFM MEDICAL INCORPORATEDDignity® Low Profile CT Port — Medical Components, Inc.DIGNITY® MINI TITANIUM CT P — Medical Components, Inc.DIGNITY® — Medical Components, Inc.Deltec — ICU MEDICAL, INC.Pro-Fuse® CT Port — Medical Components, Inc.ARROW — TELEFLEX INCORPORATEDBioFlo Vortex — Angiodynamics, Inc.DIGNITY® — Medical Components, Inc.Dignity® Mid-Sized CT Port — Medical Components, Inc.Deltec — ICU MEDICAL, INC.PowerPort ClearVUE — Bard Access Systems, Inc.Deltec — ICU MEDICAL, INC.ARROW — TELEFLEX INCORPORATEDDeltec — ICU MEDICAL, INC.Deltec — ICU MEDICAL, INC.
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2026-04-21 | ARROW INTERNATIONAL, LLC | Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality iss |
| 2025-07-21 | B.Braun Medical S.A.S. | The potential for minor injury such as damage to the vessel and/or tearing of the vessel wall. |
| 2025-02-13 | Smiths Medical ASD, Inc. | The plastic port housing and port reservoir of the ProPort Plastic Implantable Ports may separate because of a manufacturing defect. |
| 2025-02-13 | Smiths Medical ASD, Inc. | The plastic port housing and port reservoir of the ProPort Plastic Implantable Ports may separate because of a manufacturing defect. |
| 2025-02-13 | Smiths Medical ASD, Inc. | The plastic port housing and port reservoir of the ProPort Plastic Implantable Ports may separate because of a manufacturing defect. |
| 2025-02-13 | Smiths Medical ASD, Inc. | The plastic port housing and port reservoir of the ProPort Plastic Implantable Ports may separate because of a manufacturing defect. |
| 2025-02-13 | Smiths Medical ASD, Inc. | The plastic port housing and port reservoir of the ProPort Plastic Implantable Ports may separate because of a manufacturing defect. |
| 2025-02-13 | Smiths Medical ASD, Inc. | The plastic port housing and port reservoir of the ProPort Plastic Implantable Ports may separate because of a manufacturing defect. |
| 2025-02-13 | Smiths Medical ASD, Inc. | The plastic port housing and port reservoir of the ProPort Plastic Implantable Ports may separate because of a manufacturing defect. |
| 2025-02-13 | Smiths Medical ASD, Inc. | The plastic port housing and port reservoir of the ProPort Plastic Implantable Ports may separate because of a manufacturing defect. |
Query this across every FDA database — by API.
Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.
Get your free API keyRead the docsSourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.