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  document.write("<tr><td class=\"itym\" colspan=\"2\"><a href=\"https://webarchive.library.unt.edu/eot2008/20090511174450/http://www.fda.gov/cdrh/recalls/recall-042709.html\">Class I Medical Device Recall: Biosite Incorporated, Triage Cardiac Panel</a> (5/7/2009)</td></td></tr><tr><td class=\"itymrss\" colspan=\"2\">Reason for Recall: The use of the affected lot may lead to false negative results with patient samples containing troponin I at very low levels, CK-MB, and myoglobin, possibly resulting in missed or incorrect diagnosis.</td></tr>");

  
  
  
  
  document.write("<tr><td class=\"itym\" colspan=\"2\"><a href=\"https://webarchive.library.unt.edu/eot2008/20090511174450/http://www.fda.gov/cdrh/recalls/recall-020209.html\">Class I Medical Device Recall: Teleflex Medical, Arrow International Inc. 30, 40, and 50 cc Intra-Aortic Balloons</a> (4/15/2009)</td></td></tr><tr><td class=\"itymrss\" colspan=\"2\">Reason for Recall: The faulty connector of the pump tubing assembly may result in the volume setting on the pump to default to 2.5 ccs or 5 ccs (depending on the Intra-Aortic Balloon Pump model) rather than the appropriate 30, 40, or 50 cc volume.</td></tr>");

  
  
  
  
  document.write("<tr><td class=\"itym\" colspan=\"2\"><a href=\"https://webarchive.library.unt.edu/eot2008/20090511174450/http://www.fda.gov/cdrh/recalls/recall-021209b.html\">Class I Medical Device Recall: ZOLL Medical Corporation, ZOLL AED Plus Defibrillator</a> (4/8/2009)</td></td></tr><tr><td class=\"itymrss\" colspan=\"2\">This device is used by emergency or medical personnel, by others who have completed CPR AED training courses, or the public at large. It is intended to treat patients having a heart attack (cardiac arrest).</td></tr>");