Home » FDA Issues Medical Device Recall for Chronic Hemodialysis Catheters
FDA Issues Medical Device Recall for Chronic Hemodialysis Catheters
The FDA is issuing a Class I recall for Arrow International’s Arrow NextStep Antegrade Chronic Hemodialysis Catheter. There is a possibility of breakage and/or separation of the stylet within the catheters.
Upcoming Events
-
25Apr
-
07May
-
14May
-
30May