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U.S. Department of Health and Human Services

Medical Device Recalls
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21 to 30 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-1658-2024 - Expo 5F Selective Angiographic Catheters, MODEL - 5F EXPO FL4.5 (5PK), REF H74908526232; cardiac catheter 1 05/10/2024 Boston Scientific Corporation
Z-1659-2024 - Expo 5F Selective Angiographic Catheters, MODEL - 5F EXPO FL5 125CM (5PK), REF H749085262352; cardiac catheter 1 05/10/2024 Boston Scientific Corporation
Z-1660-2024 - Expo 5F Selective Angiographic Catheters, MODEL - 5F EXPO IM 125CM (5PK), REF H749085262402; 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-1662-2024 - Expo 5F Selective Angiographic Catheters, MODEL - 5F EXPO FL6 (5PK), REF H74908526252; cardiac catheter 1 05/10/2024 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 Boston Scientific Corporation
Z-1664-2024 - Expo 5F Selective Angiographic Catheters, MODEL - 5F EXPO JIG4 (5PK), REF H749085262532; cardiac catheter 1 05/10/2024 Boston Scientific Corporation
Z-1665-2024 - Expo 5F Selective Angiographic Catheters, MODEL - 5F EXPO MULTIPACK (SGL), REF H749085263001; cardiac catheter 1 05/10/2024 Boston Scientific Corporation
Z-1666-2024 - Expo 5F Selective Angiographic Catheters, MODEL - 5F EXPO MULTIPACK (5PKX3), REF H749085263002; 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
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