MD&M East

Teleflex Arrow FiberOptix and UltraFlex (IAB) Catheter Kits Recall Identified as FDA Class I

Teleflex and its subsidiary Arrow International recently received FDA Class I designation for its recall of the Arrow FiberOptix and UltraFlex Intra-Aortic Balloon (IAB) catheter kits after reporting ...
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 ...