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U.S. Department of Health and Human Services

Medical Device Recalls
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41 to 48 of 48 Results
Related Medical Device Recalls
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Product Description
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Class
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FDA Recall
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Z-1678-2024 - Expo 5F Selective Angiographic Catheters, MODEL - 5F EXPO CLS3.5 (5PK), REF H74908526574A2; cardiac catheter 1 05/10/2024 Boston Scientific Corporation
Z-1679-2024 - Expo 5F Selective Angiographic Catheters, MODEL - 5F EXPO CLS4 (5PK), REF H74908526575A2; cardiac catheter 1 05/10/2024 Boston Scientific Corporation
Z-1680-2024 - Expo 5F Selective Angiographic Catheters, MODEL - 5F EXPO AR1 (5PK), REF H74908526842; cardiac catheter 1 05/10/2024 Boston Scientific Corporation
Z-1681-2024 - Expo 5F Selective Angiographic Catheters, MODEL - 5F EXPO AR2 (5PK), REF H74908526862; cardiac catheter 1 05/10/2024 Boston Scientific Corporation
Z-1682-2024 - Expo 5F Selective Angiographic Catheters, MODEL - 5F EXPO AR MOD (5PK), REF H74908526892; cardiac catheter 1 05/10/2024 Boston Scientific Corporation
Z-1683-2024 - Expo 5F Selective Angiographic Catheters, MODEL - 5F EXPO AL1 (5PK), REF H74908526962; cardiac catheter 1 05/10/2024 Boston Scientific Corporation
Z-1684-2024 - Expo 5F Selective Angiographic Catheters, MODEL - 5F EXPO AL2 (5PK), REF H74908526982; cardiac catheter 1 05/10/2024 Boston Scientific Corporation
Z-1639-2024 - Expo 5F Selective Angiographic Catheters, MODEL - 5F EXPO FR4 (5PK), REF H74908526022; cardiac catheter 1 05/10/2024 Boston Scientific Corporation
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