Teleflex has recalled nearly 335,000 catheterization kits from the U.S. after discovering an issue linked to 10 injuries and one death, the Food and Drug Administration said Wednesday. The company ...

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 ...

Teleflex and its subsidiary Arrow International have initiated a recall of specific intra-aortic balloon (IAB) catheter kits due to a manufacturing defect that may prevent full balloon inflation, ...

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

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 ...

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 ...

Teleflex is recalling International Intra-Aortic Balloon Catheter Kits and Percutaneous Insertion Kits, according to an FDA press release on Friday. The recall is considered by the FDA as a Class 1.

Struggling Teleflex ($TFX) in February warned of an impending restructuring plan that will involve the usual mix of layoffs, relocations and outsourcing. The Wayne ...

DUBLIN, April 27, 2021 /PRNewswire/ -- Medtronic plc (NYSE:MDT), the global leader in medical technology, today announced it has received Breakthrough Device Designation status from the U.S. Food and ...