
Teleflex and its subsidiary Arrow International have recalled the Arrow QuickFlash radial artery and radial artery/arterial line catheterization kits due to a potentially defective component that could cause arterial vasospasm and vessel injury, posing a serious risk of injury or death.


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The Class I recall stems from reports of increased resistance in the guidewire handle and chamber during use, which could cause injury to the blood vessel walls.

Arrow QuickFlash Radial Artery Catheterization Kits Recalled

teleflex-and-arrow-international-recall-arrow-quickflash-radial-artery-catheterization-kits-due-to-potential-guidewire-defect-and-risk-of-serious-injury-or-death


Teleflex and Arrow International Recall Arrow QuickFlash Radial Artery Catheterization Kits Due to Potential Guidewire Defect and Risk of Serious Injury or Death
