The IAB catheter kits are typically used in conjunction with a balloon pump. Credit: MAD.vertise / Shutterstock. Teleflex and its subsidiary Arrow International have initiated a recall of specific ...

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(New England Journal of Medicine) Arrow QuickFlash radial artery and radial artery/arterial line catheterization kits are under class I recall due to reports of increased resistance in the ...

The U.S. Food and Drug Administration (FDA) has announced on April 3 that Teleflex and Arrow International are recalling the ARROW QuickFlash Radial Artery and Radial Artery/Arterial Line ...

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.

Affected kits may cause injury to the vessel wall, vasospasm, embolism or death. Arrow International, a subsidiary of Teleflex, has issued a recall of its radial artery and arterial line ...

The associated devices are the Arrow QuickFlash Radial Artery and Radial Artery/Arterial Line Catheterization Kits which enable clinicians access to a patient’s peripheral arterial circulation or ...

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When normal individuals are asked to localize and mark the midpoint of a radial line, they tend to bisect it farther than the true center. It has been suggested that radial misbisection depends on the ...