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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 10 of 13 Results
Recall Date to: 04/27/2015 PMA Number: P910077
 
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Guidant ENDOTAK SQ Array models 0048, 0049, 0085. Subcutaneous Lead Array. Cardioversion/Defibrill... 2 08/30/2005 Guidant Corporation
Guidant Zoom Latitude Programming System, Model 3120, Programmer/Recorder/Monitor (PRM). A portable... 3 10/12/2006 Guidant Corporation
Guidant LATITUDE® Communicator, model 6481, Boston Scientific 4100 Hamline Avenue North, St. Paul, M... 2 11/12/2009 Boston Scientific CRM Corp
Boston Scientific, LATITUDE® Communicator, Distributed by Boston Scientific, 4100 Hamline Avenue Nor... 2 05/20/2010 Boston Scientific CRM Corp
Boston Scientific's LATITUDE Patient Management System: LATITUDE 6.1 Patient Management System We... 2 04/26/2011 Boston Scientific CRM Corp
LATITUDE® Patient Management System Communicator, Model 6482. The LATITUDE Patient Management sys... 2 09/09/2011 Boston Scientific CRM Corp
Boston Scientific, LATITUDE® Patient Management System Communicator, Model 6476, Distributed by B... 3 09/28/2011 Boston Scientific CRM Corp
LATITUDE® Paceart Integration Software, version 1.00 Model 6472. LATITUDE Paceart Integration is ... 2 10/12/2011 Boston Scientific CRM Corp
LATITUDE® Patient Management System, Models 6441*, 6442*, 6465*, 6488 (USA). There are two softwa... 2 12/01/2011 Boston Scientific CRM Corp
LATITUDE Patient management System, Model 6488, software version 7.2. It is indicated for use to rem... 3 02/23/2012 Boston Scientific CRM Corp
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