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U.S. Department of Health and Human Services

Medical Device Recalls

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31 to 40 of 48 Results
Related Medical Device Recalls
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Product Description
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FDA Recall
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Z-1650-2024 - Expo 5F Selective Angiographic Catheters, MODEL - 5F EXPO IMT (5PK), REF H749085262022; cardiac catheter 1 05/10/2024 FEI # 3002095335
Boston Scientific Corporation
Z-1663-2024 - Expo 5F Selective Angiographic Catheters, MODEL - 5F EXPO JIG3.5 (5PK), REF H749085262522; cardiac catheter 1 05/10/2024 FEI # 3002095335
Boston Scientific Corporation
Z-1664-2024 - Expo 5F Selective Angiographic Catheters, MODEL - 5F EXPO JIG4 (5PK), REF H749085262532; cardiac catheter 1 05/10/2024 FEI # 3002095335
Boston Scientific Corporation
Z-1646-2024 - Expo 5F Selective Angiographic Catheters, MODEL - 5F EXPO KIMNY (5PK), REF H749085261802; cardiac catheter 1 05/10/2024 FEI # 3002095335
Boston Scientific Corporation
Z-1648-2024 - Expo 5F Selective Angiographic Catheters, MODEL - 5F EXPO LCB (5PK), REF H749085261952; cardiac catheter 1 05/10/2024 FEI # 3002095335
Boston Scientific Corporation
Z-1666-2024 - Expo 5F Selective Angiographic Catheters, MODEL - 5F EXPO MULTIPACK (5PKX3), REF H749085263002; cardiac catheter 1 05/10/2024 FEI # 3002095335
Boston Scientific Corporation
Z-1665-2024 - Expo 5F Selective Angiographic Catheters, MODEL - 5F EXPO MULTIPACK (SGL), REF H749085263001; cardiac catheter 1 05/10/2024 FEI # 3002095335
Boston Scientific Corporation
Z-1668-2024 - Expo 5F Selective Angiographic Catheters, MODEL - 5F EXPO MULTIPACK 145 (5PKX3), REF H749085263012; cardiac catheter 1 05/10/2024 FEI # 3002095335
Boston Scientific Corporation
Z-1670-2024 - Expo 5F Selective Angiographic Catheters, MODEL - 5F EXPO MULTIPACK 145 (5PKX3), REF H749085265002; cardiac catheter 1 05/10/2024 FEI # 3002095335
Boston Scientific Corporation
Z-1673-2024 - Expo 5F Selective Angiographic Catheters, MODEL - 5F EXPO MULTIPACK 145 (5PKX3), REF H749085265022; cardiac catheter 1 05/10/2024 FEI # 3002095335
Boston Scientific Corporation
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