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ARROW
TELEFLEX INCORPORATED · Model IPN036753 · UDI-DI 30801902123726
LJS
Prescription
1
510(k) clearances
36,803
Adverse events (128 deaths)
332
Recalls
89
Facilities
Description
Arrow(R) PICC powered by Arrow(R) VPS(R) Stylet
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 experience leaking a |
| 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 experience leaking a |
| 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 supplier. |
| 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 supplier. |
| 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 supplier. |
| 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 supplier. |
| 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 supplier. |
| 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 issues and limited repo |
| 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 lead to increased mater |
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Get your free API keyRead the docsData compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.