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
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Z-2450-2012 - Armada 35/ Armada 35 LL PTA Catheters. The device is intended for dilatation of lesions in the vasculature. | 2 | 09/25/2012 |
FEI # 2024168 Abbott Vascular |
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