Healio

FDA designates recall of central venous access, catheter kits as class I

Please provide your email address to receive an email when new articles are posted on . The FDA announced that Teleflex and Arrow International LLC are recalling both the Arrow MAC Two-Lumen Central ...
Yahoo Finance

Teleflex and Arrow recall IAB catheter kits due to risk of injury or death

Teleflex and its subsidiary Arrow International have initiated a recall of specific intra-aortic balloon (IAB) catheter kits due to a manufacturing defect that may prevent full balloon inflation, ...
Healio

Two intra-aortic balloon catheter kits recalled; three deaths reported

Please provide your email address to receive an email when new articles are posted on . The recall of two varieties of intra-aortic balloon catheter kits has been ...
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 ...
Nature

Incidence of Catheter Related Bloodstream Infections After The Removal of Percutaneous Intravenous Catheters in Preterm Infants.

The use of PICC lines in preterm infants increases the risk for systemic bacterial infections. The overall incidence of Catheter Related Bloodstream Infection (CRBSI) after PICC line removal is not ...