Becker's Hospital Review

Catheterization kits recalled after 10 injuries, 1 death: FDA

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 ...
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 ...
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 ...
MD&M East

Teleflex, Arrow International Recall Arrow QuickFlash Radial Artery and Radial Artery/Arterial Line Catheterization Kits

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 ...
Business Insider

Centurion's smART Kit for Radial Arterial Catheterization Newest Clinician-Driven Vascular Access Solution

WILLIAMSTON, Mich., March 15, 2017 /PRNewswire/ -- Centurion Medical Products, a leader in medical product innovation and global patient care, is launching its new smART™ Kit for radial arterial ...