Home › Device types › LJS
Catheter, Intravascular, Therapeutic, Long-Term Greater Than 30 Days
FDA product code LJS · Class 2 · General Hospital
5,601
Registered devices
37,274
Adverse events
332
Recalls
302
510(k) clearances
Devices with this code
ARROW — TELEFLEX INCORPORATEDARROW — TELEFLEX INCORPORATEDPowerPICC SOLO — Bard Access Systems, Inc.PowerPICC Provena — Bard Access Systems, Inc.BioFlo — NAVILYST MEDICAL, INC.Leonard — Bard Access Systems, Inc.Groshong — Bard Access Systems, Inc.HydroPICC Basic Kit (130cm GW) — Access Vascular, Inc.NAUTILUS DELTA — Bard Access Systems, Inc.MIDLINE CATHETER — Medical Components, Inc.PowerPICC — Bard Access Systems, Inc.Xcela — NAVILYST MEDICAL, INC.Xcela — NAVILYST MEDICAL, INC.ARROW — TELEFLEX INCORPORATEDARROW — TELEFLEX INCORPORATEDCook Spectrum Turbo-Ject — COOK INCORPORATEDARROW — TELEFLEX INCORPORATEDMedline Industries, Inc. — MEDLINE INDUSTRIES, INC.C3 WAVE SYSTEM — Medical Components, Inc.PICC-NATE — UTAH MEDICAL PRODUCTS, INC.BioFlo — NAVILYST MEDICAL, INC.BioFlo — NAVILYST MEDICAL, INC.PRO-PICC® CT — Medical Components, Inc.Xcela — NAVILYST MEDICAL, INC.
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2026-06-15 | Argon Medical Devices, Inc | Catheters, indicated for short/long-term peripheral access to central venous system for the administration of fluids, medications, nutrients; and sampling, may |
| 2026-06-15 | Argon Medical Devices, Inc | Catheters, indicated for short/long-term peripheral access to central venous system for the administration of fluids, medications, nutrients; and sampling, may |
| 2026-05-21 | Bard Access Systems, Inc. | Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplie |
| 2026-05-21 | Bard Access Systems, Inc. | Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplie |
| 2026-05-21 | Bard Access Systems, Inc. | Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplie |
| 2026-05-21 | Bard Access Systems, Inc. | Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplie |
| 2026-05-21 | Bard Access Systems, Inc. | Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplie |
| 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 |
| 2025-12-12 | Bard Peripheral Vascular Inc | Due to damage to outer tray that can potentially compromise the sterile barrier |
| 2025-03-11 | Bard Access Systems, Inc. | Catheters indicated for short-or-long term access to the central venous system have tubing that exceeded melt flow index specification (higher), which could lea |
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