Medical Device Recalls
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31 to 31 of 31 Results
PMA Number: P980035 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Medtronic, Kappa 600 KDR600,KDR601,KDR603,KDR606,KDR651,KDR653 The devices are implantable pulse... | 2 | 04/29/2011 |
FEI # 2182208 Medtronic Inc. Cardiac Rhythm Disease Management |
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