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Product Description
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Recall Class
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FDA Recall Posting Date
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Recalling Firm
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Z-1668-2024 - Expo 5F Selective Angiographic Catheters, MODEL - 5F EXPO MULTIPACK 145 (5PKX3), REF H749085263012; cardiac catheter
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1
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05/10/2024
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FEI # 3002095335 Boston Scientific Corporation
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Z-1665-2024 - Expo 5F Selective Angiographic Catheters, MODEL - 5F EXPO MULTIPACK (SGL), REF H749085263001; cardiac catheter
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1
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05/10/2024
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FEI # 3002095335 Boston Scientific Corporation
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Z-1666-2024 - Expo 5F Selective Angiographic Catheters, MODEL - 5F EXPO MULTIPACK (5PKX3), REF H749085263002; cardiac catheter
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1
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05/10/2024
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FEI # 3002095335 Boston Scientific Corporation
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Z-1648-2024 - Expo 5F Selective Angiographic Catheters, MODEL - 5F EXPO LCB (5PK), REF H749085261952; cardiac catheter
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1
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05/10/2024
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FEI # 3002095335 Boston Scientific Corporation
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Z-1646-2024 - Expo 5F Selective Angiographic Catheters, MODEL - 5F EXPO KIMNY (5PK), REF H749085261802; cardiac catheter
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1
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05/10/2024
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FEI # 3002095335 Boston Scientific Corporation
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Z-1664-2024 - Expo 5F Selective Angiographic Catheters, MODEL - 5F EXPO JIG4 (5PK), REF H749085262532; cardiac catheter
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1
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05/10/2024
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FEI # 3002095335 Boston Scientific Corporation
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Z-1663-2024 - Expo 5F Selective Angiographic Catheters, MODEL - 5F EXPO JIG3.5 (5PK), REF H749085262522; cardiac catheter
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1
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05/10/2024
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FEI # 3002095335 Boston Scientific Corporation
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Z-1650-2024 - Expo 5F Selective Angiographic Catheters, MODEL - 5F EXPO IMT (5PK), REF H749085262022; cardiac catheter
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1
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05/10/2024
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FEI # 3002095335 Boston Scientific Corporation
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Z-1651-2024 - Expo 5F Selective Angiographic Catheters, MODEL - 5F EXPO IMC (5PK), REF H749085262032; cardiac catheter
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1
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05/10/2024
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FEI # 3002095335 Boston Scientific Corporation
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Z-1660-2024 - Expo 5F Selective Angiographic Catheters, MODEL - 5F EXPO IM 125CM (5PK), REF H749085262402; cardiac catheter
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1
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05/10/2024
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FEI # 3002095335 Boston Scientific Corporation
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