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U.S. Department of Health and Human Services

Medical Device Recalls

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Product Description
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Class
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FDA Recall
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Recalling Firm
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Expo 5F Selective Angiographic Catheters, MODEL - 5F EXPO MULTIPACK 155 (5PKX3), REF H749085263022; ... 1 05/10/2024 Boston Scientific Corporation
Expo 5F Selective Angiographic Catheters, MODEL - 5F EXPO MULTIPACK 145 (5PKX3), REF H749085265002; ... 1 05/10/2024 Boston Scientific Corporation
Expo 5F Selective Angiographic Catheters, MODEL - 5F EXPO WR (SGL), REF H74908526501; cardiac cathe... 1 05/10/2024 Boston Scientific Corporation
Expo 5F Selective Angiographic Catheters, MODEL - 5F EXPO WR (5PK), REF H74908526502; cardiac cathe... 1 05/10/2024 Boston Scientific Corporation
Expo 5F Selective Angiographic Catheters, MODEL - 5F EXPO MULTIPACK 145 (5PKX3), REF H749085265022; ... 1 05/10/2024 Boston Scientific Corporation
Expo 5F Selective Angiographic Catheters, MODEL - 5F EXPO WRP (SGL), REF H74908526511; cardiac cath... 1 05/10/2024 Boston Scientific Corporation
Expo 5F Selective Angiographic Catheters, MODEL - 5F EXPO WRP (5PK), REF H74908526512; cardiac cath... 1 05/10/2024 Boston Scientific Corporation
Expo 5F Selective Angiographic Catheters, MODEL - 5F EXPO CLS2.5 (5PK), REF H74908526572A2; cardiac... 1 05/10/2024 Boston Scientific Corporation
Expo 5F Selective Angiographic Catheters, MODEL - 5F EXPO CLS3 (5PK), REF H74908526573A2; cardiac c... 1 05/10/2024 Boston Scientific Corporation
Expo 5F Selective Angiographic Catheters, MODEL - 5F EXPO CLS3.5 (5PK), REF H74908526574A2; cardiac... 1 05/10/2024 Boston Scientific Corporation

*   The maximium 500 devices meeting your search criteria returned. Please narrow your search.
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