Medical Device Recalls
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11 to 13 of 13 Results
Recall Date to: 07/28/2014 PMA Number: P910077 |
Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Guidant LATITUDE® Communicator, model 6481, Boston Scientific 4100 Hamline Avenue North, St. Paul, M... | 2 | 11/12/2009 | Boston Scientific CRM Corp |
Guidant Zoom Latitude Programming System, Model 3120, Programmer/Recorder/Monitor (PRM). A portable... | 3 | 10/12/2006 | Guidant Corporation |
Guidant ENDOTAK SQ Array models 0048, 0049, 0085. Subcutaneous Lead Array. Cardioversion/Defibrill... | 2 | 08/30/2005 | Guidant Corporation |
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