Medical Device Recalls
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1 result found
Related Medical Device Recalls |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Z-0729-04 - Impulse 5F 145 (degree) Multipack Angiographic Catheters, Catalog Number H749163913011 | 2 | 07/20/2004 |
FEI # 3002095335 Boston Scientific Scimed |
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