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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
Product: expo Recall Date from: 03/01/2024
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Expo 5F Selective Angiographic Catheters, MODEL - 5F EXPO CLS3.5 (5PK), REF H74908526574A2; cardiac... 1 05/10/2024 FEI # 3002095335
Boston Scientific Corporation
Expo 5F Selective Angiographic Catheters, MODEL - 5F EXPO CLS4 (5PK), REF H74908526575A2; cardiac c... 1 05/10/2024 FEI # 3002095335
Boston Scientific Corporation
Expo 5F Selective Angiographic Catheters, MODEL - 5F EXPO AR1 (5PK), REF H74908526842; cardiac cath... 1 05/10/2024 FEI # 3002095335
Boston Scientific Corporation
Expo 5F Selective Angiographic Catheters, MODEL - 5F EXPO AR2 (5PK), REF H74908526862; cardiac cath... 1 05/10/2024 FEI # 3002095335
Boston Scientific Corporation
Expo 5F Selective Angiographic Catheters, MODEL - 5F EXPO AR MOD (5PK), REF H74908526892; cardiac c... 1 05/10/2024 FEI # 3002095335
Boston Scientific Corporation
Expo 5F Selective Angiographic Catheters, MODEL - 5F EXPO AL1 (5PK), REF H74908526962; cardiac cath... 1 05/10/2024 FEI # 3002095335
Boston Scientific Corporation
Expo 5F Selective Angiographic Catheters, MODEL - 5F EXPO AL2 (5PK), REF H74908526982; cardiac cath... 1 05/10/2024 FEI # 3002095335
Boston Scientific Corporation
Expo 5F Selective Angiographic Catheters, MODEL - 5F EXPO FR4 (5PK), REF H74908526022; cardiac cathe... 1 05/10/2024 FEI # 3002095335
Boston Scientific Corporation
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