Teleflex Inc.

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The Arrow FiberOptix and UltraFlex Intra-Aortic Balloon (IAB) Catheter Kits are being recalled for manufacturing issues that may prevent full balloon inflation and cause patient harm
News | Balloon Catheter
FDA Announces Teleflex/Arrow International Recall Arrow FiberOptix and UltraFlex Intra-Aortic Balloon (IAB) Catheter Kits

June 13, 2024 — The U.S. Food and Drug Administration (FDA) announced that Teleflex, and their subsidiary Arrow ...

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Company expands structural heart portfolio and begins the limited market release of a bipolar temporary pacing guidewire
News | Guidewires
Teleflex Announces the Limited Market Release of the Wattson Temporary Pacing Guidewire

May 6, 2024 — Teleflex Incorporate, a leading global provider of medical technologies, today announced that the Wattson ...

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The FDA has identified this as a Class I recall, the most serious type of recall. Use of these devices may cause serious injuries, serious health consequences, or death
News | Catheters
FDA Announces Teleflex and Arrow International Recall of ARROW QuickFlash Radial Artery and Radial Artery/Arterial Line Catheterization Kits for Increased Resistance That May Lead to Vessel Injuries, Narrowing, or Blockage

April 3, 2024 — The U.S. Food and Drug Administration (FDA) announced that Teleflex and Arrow International are ...

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The FDA has identified this as a Class I recall, the most serious type of recall. Use of these devices may cause serious injuries or death.
News | FDA
Teleflex, and Arrow International, Recall Pressure Injectable Catheter Kits for Mislabeling

November 7, 2023 — The U.S. Food and Drug Administration (FDA) announced that Teleflex, and its subsidiary Arrow ...

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Teleflex and Arrow International recall ARROW endurance extended dwell peripheral catheter system due to risk of catheter separation and leakage
News | Catheter
Teleflex and Arrow International Recall ARROW Endurance Extended Dwell Peripheral Catheter System

June 26, 2023 — The U.S. Food and Drug Administration (FDA) has issued a Class I recall on the Teleflex and Arrow ...

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Arrow International, LLC, a Subsidiary of Teleflex, Inc, recalls Arrow AutoCAT 2, AC3 intra-aortic balloon pumps for unexpectedly short battery run times
Feature | Intra-Aortic Balloon Pumps (IABP)
Teleflex Recalls Arrow Intra-Aortic Balloon Pumps for Short Battery

The U.S. Food and Drug Administration (FDA) has issued a Class I recall on the Arrow AutoCAT 2 and AC3 Intra-Aortic ...

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TrapLiner Catheter
News | Catheter
Teleflex Receives FDA Clearance for Expanded Indication for Specialty Catheter and Coronary Guidewire Use in CTO PCI Procedures

February 25, 2022 – Teleflex Incorporated, a leading global provider of medical technologies, today announced that the U ...

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QuickClot already has an FDA-cleared product for use for vascular access hemostasis management in cath lab procedures. The hemostatic technology consists of a non-woven material impregnated with kaolin, an inorganic mineral. When kaolin contacts blood it activates Factor XII, which accelerates the body’s natural clotting cascade.
News | Hemostasis Management
Teleflex Completes Enrollment in IDE Study of QuickClot in Cardiac Surgery

October 27, 2021 — Teleflex Inc. announced the completion of patient enrollment in a clinical study evaluating the ...

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Teleflex Acquires Essential Medical
News | Vascular Closure Devices
Teleflex Acquires Essential Medical

October 5, 2018 — Teleflex Inc. announced the acquisition of Essential Medical Inc. Based in Exton, Pa., Essential ...

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Teleflex Launches Next-Generation Sympro Elite and Expro Elite Snares
Technology | Cath Lab
Teleflex Launches Next-Generation Sympro Elite and Expro Elite Snares

February 7, 2018 — Teleflex Inc. has announced 510(k) clearance by the U.S. Food and Drug Administration (FDA) and U.S ...

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