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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 10 of 48 Results
Related Medical Device Recalls
 
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Product Description
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Class
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FDA Recall
Posting Date
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Z-1674-2024 - Expo 5F Selective Angiographic Catheters, MODEL - 5F EXPO WRP (SGL), REF H74908526511; cardiac catheter 1 05/10/2024 Boston Scientific Corporation
Z-1675-2024 - Expo 5F Selective Angiographic Catheters, MODEL - 5F EXPO WRP (5PK), REF H74908526512; cardiac catheter 1 05/10/2024 Boston Scientific Corporation
Z-1671-2024 - Expo 5F Selective Angiographic Catheters, MODEL - 5F EXPO WR (SGL), REF H74908526501; cardiac catheter 1 05/10/2024 Boston Scientific Corporation
Z-1672-2024 - Expo 5F Selective Angiographic Catheters, MODEL - 5F EXPO WR (5PK), REF H74908526502; cardiac catheter 1 05/10/2024 Boston Scientific Corporation
Z-1661-2024 - Expo 5F Selective Angiographic Catheters, MODEL - 5F EXPO TIG4 (5PK), REF H749085262502; cardiac catheter 1 05/10/2024 Boston Scientific Corporation
Z-1647-2024 - Expo 5F Selective Angiographic Catheters, MODEL - 5F EXPO RCB (5PK), REF H749085261902; cardiac catheter 1 05/10/2024 Boston Scientific Corporation
Z-1669-2024 - Expo 5F Selective Angiographic Catheters, MODEL - 5F EXPO MULTIPACK 155 (5PKX3), REF H749085263022; cardiac catheter 1 05/10/2024 Boston Scientific Corporation
Z-1667-2024 - Expo 5F Selective Angiographic Catheters, MODEL - 5F EXPO MULTIPACK 145 (SGL), REF H749085263011; cardiac catheter 1 05/10/2024 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 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 Boston Scientific Corporation
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