Medscape

Arrow QuickFlash Radial Artery Catheterization Kits Recalled

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 ...
TCTMD

Class I Recall for 330,000 Radial Artery Catheterization Kits: FDA

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 ...
Healio

FDA designates recall of radial artery and arterial line catheterization kits as class I

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 ...
MedPage Today

Radial Cath Kits Recalled; siRNAs for Lipid Lowering; Smartphone HF Detection

In the DEDICATE-DZHK6 population, designed to be more reflective of routine clinical practice, transcatheter aortic valve replacement matched surgery for outcomes at 1 year among people at low or ...