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FDA Announces Teleflex/Arrow International Recall Arrow FiberOptix and UltraFlex Intra-Aortic Balloon (IAB) Catheter Kits

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

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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

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
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Teleflex, and Arrow International, Recall Pressure Injectable Catheter Kits for Mislabeling

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.

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Teleflex and Arrow International Recall ARROW Endurance Extended Dwell Peripheral Catheter System

Teleflex and Arrow International recall ARROW Endurance Extended Dwell peripheral catheter system due to risk of catheter separation and leakage

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Teleflex Recalls Arrow Intra-Aortic Balloon Pumps for Short Battery

Arrow International, LLC, a Subsidiary of Teleflex, Inc, recalls Arrow AutoCAT 2, AC3 intra-aortic balloon pumps for unexpectedly short battery run times

Emergency departmentTeleflex incRoom serviceDrug administrationVascular access serviceCatheter labTeleflex customer serviceHarrow internationalAortic balloonRecall databaseArrow intra aortic balloon pumpsAortic balloon pumpsUrgent medical device notificationAcknowledgement formTeleflex customer