FDA Device recall Z-2970-2024
Impella 5.5 SmartAssist S2 Set, JP
- FDA Device
- Class II
- ongoing
- Published 2024-09-11
On 2024-09-11 the FDA classified a Class II recall of Impella 5.5 SmartAssist S2 Set, JP by Abiomed, citing A potential device interaction between the Shockwave Coronary IVL Catheter and left-sided Impella Pumps during coronary interventions. Currently there is no Abiomed labeling (IFU….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2970-2024 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2024-08-05 |
| Published | 2024-09-11 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | Abiomed |
| Distribution | US |
Product
Impella 5.5 SmartAssist S2 Set, JP; Product Code: 1000459;
Reason
A potential device interaction between the Shockwave Coronary IVL Catheter and left-sided Impella Pumps during coronary interventions. Currently there is no Abiomed labeling (IFU etc.) content related to this potential interaction, so Abiomed will update the IFU to include information on this potential device interaction.
Identifiers
| code_info | Product Code: 1000459; UDI-DI: 00813502013054; Serial Numbers: 491248 491249 491975 491974 490744 491976 491977 490747…Product Code: 1000459; UDI-DI: 00813502013054; Serial Numbers: 491248 491249 491975 491974 490744 491976 491977 490747 490725 490739 490740 490741 490742 490743 490727 491252 491239 491253 491235 491241 492012 490724 492009 491246 492005 492010 492011 491981 491240 491243 493477 491982 493476 493478 493480 493479 492004 490745 494684 494686 494687 493837 493838 493839 494689 494688 494690 494691 494692 494693 490746 494734 491236 494736 493836 494735 499143 494737 494738 491242 493840 492013 499157 499148 499156 491237 491978 494743 499153 499144 501038 501071 499155 499150 501132 499154 490728 499152 499168 501040 499738 499744 499170 501183 499740 499739 499741 501186 501041 499743 499746 501093 501205 492008 499742 501097 501094 501128 501129 501130 501184 501131 501054 491245 501204 504904 501039 501057 499147 501069 501070 501207 501213 501215 501187 498548 491238 498549 498930 501217 501072 501206 504888 491979 507422 504890 494740 504891 504893 501042 499745 499747 501056 501185 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:57 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2970-2024%22
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