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 ...

Compared with conventional training, simulator training shortens the learning curve and produces superior performance among electrophysiology fellows learning transseptal catheterization, according to ...