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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 10 of 18 Results
Related Medical Device Recalls
 
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Z-2954-2024 - Impella CP Smart Assist Set, EU; Product Code: 0048-0014; 2 09/04/2024 FEI # 1220648
Abiomed, Inc.
Z-2971-2024 - Impella 5.5 with SmartAssist S2 Set, EU; Product Code: 1000482; 2 09/04/2024 FEI # 1220648
Abiomed, Inc.
Z-2956-2024 - Impella CP Pump Set, Japan; Product Code: 0048-0034-JP; 2 09/04/2024 FEI # 1220648
Abiomed, Inc.
Z-2957-2024 - Impella CP Pump 371 Set, Clinical Trial; Product Code: 0048-0040; 2 09/04/2024 FEI # 1220648
Abiomed, Inc.
Z-2958-2024 - Impella CP Smart Assist Set, Canada; Product Code: 0048-0044; 2 09/04/2024 FEI # 1220648
Abiomed, Inc.
Z-2959-2024 - Pump 371 14F LT CMR Set; Product Code: 0048-0045; 2 09/04/2024 FEI # 1220648
Abiomed, Inc.
Z-2960-2024 - Impella CP Smart Assist Set APAC; Product Code: 0048-0047; 2 09/04/2024 FEI # 1220648
Abiomed, Inc.
Z-2961-2024 - Impella 5.5 with SmartAssist Set, EU; Product Code: 0550-0002; 2 09/04/2024 FEI # 1220648
Abiomed, Inc.
Z-2962-2024 - Impella 5.5 with SmartAssist Set, CA; Product Code: 0550-0004; 2 09/04/2024 FEI # 1220648
Abiomed, Inc.
Z-2963-2024 - Impella 5.5 with SmartAssist Set, US; Product Code: 0550-0008; 2 09/04/2024 FEI # 1220648
Abiomed, Inc.
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