TCTMD

Class I Recall for Cordis’ Super Torque Catheters with Radiopaque Markers

Cordis is recalling the Super Torque MB angiographic catheter with radiopaque marker bands, the US Food and Drug Administration announced this week, categorizing the action as a class I recall, the ...
Medscape

FDA Class 1 Recall of Imager II Angiographic Catheters

Boston Scientific is recalling their Imager II 5F angiographic catheters in the United States because the catheter tip could become detached during a patient procedure or during procedure preparation.
Healio

FDA labels Cordis’ recall of angiographic catheters as class I

Please provide your email address to receive an email when new articles are posted on . The FDA has identified Cordis’ recall of its angiographic catheter with radiopaque marker bands as Class I, the ...
Reuters

FDA Says It Has Identified Boston Scientific Corp's Imager II 5F Angiographic Catheters As A Class I Recall

* FDA -BOSTON SCIENTIFIC IS RECALLING IMAGER II 5F ANGIOGRAPHIC CATHETERS BECAUSE THERE IS POTENTIAL FOR CATHETER TIP TO DETACH DURING PATIENT PROCEDURE * FDA - THERE ARE NINE REPORTED INJURIES FROM ...