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Device manufacturer Teleflex, and its subsidiary Arrow International, are recalling certain radial artery catheterization kits following reports of malfunction in both the guidewire handle and chamber ...

Teleflex and its subsidiary Arrow International have recalled the Arrow QuickFlash radial artery and radial artery/arterial line catheterization kits over a potentially defective component. The ...

Teleflex and its subsidiary Arrow International recalled 334,995 catheter kits after receiving reports of increased resistance in the guidewire handle and chamber during use, the FDA said April 3. The ...

Please provide your email address to receive an email when new articles are posted on . The FDA designated the recall of radial artery and arterial line catheterization kits as class I, the most ...

Teleflex and its subsidiary Arrow International recently announced the Class I recall of its Arrow QuickFlash Radial Artery and Radial Artery/Arterial Line Catheterization Kits after potential ...

Please provide your email address to receive an email when new articles are posted on . The FDA announced that Teleflex and Arrow International LLC are recalling both the Arrow MAC Two-Lumen Central ...

The new Hemolung XG4 Cartridge and Catheter Kits further simplify initiation of Respiratory Dialysis ®. PITTSBURGH--(BUSINESS WIRE)--ALung Technologies, Inc., the leading provider of low-flow ...