January 28, 2008
Balloon Catheter Recall
Posted at January 28, 2008 10:51 AM in .
Johnson & Johnson is recalling approximately 132, 000 of its Dura Star RX" and "Fire Star RX PTCA balloon catheters. Johnson & Johnson's subsidiary Cordis is responsible for the manufacture of the catheters which may fail causing severe injury or even death. Apparently, there are no issues with the Johnson & Johnson cardiac stent.
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