Medical Device Recalls
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1 result found
Recall Number: Z-1669-2024 |
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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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| Expo 5F Selective Angiographic Catheters, MODEL - 5F EXPO MULTIPACK 155 (5PKX3), REF H749085263022; ... | 1 | 05/10/2024 |
FEI # 3002095335 Boston Scientific Corporation |
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