Cordis Corporation announced today a nationwide voluntary recall of all lots of the CROSSOVER™ Sheath Introducer due to complaints about stretching or fracture of the sheath during use. The CROSSOVER Sheath Introducer is a product developed and manufactured by Thomas Medical Products, Inc., and distributed by Cordis. It is a long-coil reinforced, … [Read more...]
Search Results for: catheter
Portex Uncuffed Pediatric-Sized Tracheal Tubes
Smiths Medical announced that it is initiating a nationwide voluntary recall of Portex® Uncuffed Pediatric-Sized Tracheal Tubes (sizes 2.5, 3.0 and 3.5 mm) manufactured before September 2009. Description of the Issue A small number of tubes were manufactured with internal diameters slightly smaller than indicated on the labeling, which may create … [Read more...]
Smiths Medical Issues Urgent Device Recall Of Portex Pediatric-Sized Tracheal Tubes
Smiths Medical announced that it is initiating a nationwide voluntary recall of Portex® Uncuffed Pediatric-Sized Tracheal Tubes (sizes 2.5, 3.0 and 3.5 mm) manufactured before September 2009. Description of the Issue A small number of tubes were manufactured with internal diameters slightly smaller than indicated on the labeling, which may create … [Read more...]
Urgent Medtronic Neuromodulation INDURA IP Product Recall
FDA has issued a Class I Recall on Medtronic Neuromodulation INDURA IP intrathecal catheters, sutureless pump connector revision kits and intrathecal catheter pump segment revision kits. There are potential misconnections of the Medtronic sutureless connector ("SC") catheters from the catheter port on the medtronic pump. These misconnections have … [Read more...]
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