Medical Device Recalls
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1 result found
Related Medical Device Recalls |
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Product Description
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Recall
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FDA Recall
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Recalling Firm
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Z-1607-2013 - Medtronic, Consulta® CRT-P, Model C4TR01, C3TR01 (not approved for US), and Syncra® CRT-P, Model C2TR01, Sterile EO. Dual chamber and atrial tracking modes are indicated for patients who may be... | 2 | 06/27/2013 | Medtronic Inc. Cardiac Rhythm Disease Management |
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