FDA Device recall Z-2959-2024
Pump 371 14F LT CMR Set
- FDA Device
- Class II
- ongoing
- Published 2024-09-11
On 2024-09-11 the FDA classified a Class II recall of Pump 371 14F LT CMR Set 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-2959-2024 |
| 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
Pump 371 14F LT CMR Set; Product Code: 0048-0045;
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: 0048-0045; UDI-DI: 00813502011876; Serial Numbers: 381707 379142 384464 378824 378853 383418 384433 38273…Product Code: 0048-0045; UDI-DI: 00813502011876; Serial Numbers: 381707 379142 384464 378824 378853 383418 384433 382733 384889 382279 384890 382280 384814 382281 384815 382282 382283 384816 384817 382284 384624 384625 382286 384818 384819 384820 384821 384822 384823 383689 382734 382735 383684 382736 382737 383686 382738 382739 383687 382740 383688 382741 383744 382742 383745 383520 383746 383521 383747 383522 383748 383749 383750 383751 383752 383753 383523 384891 383524 384892 382287 383525 383526 384893 381601 383527 381602 384894 383529 381604 384895 381605 384896 381606 381607 384897 381608 384898 381609 383798 381610 383799 383801 381325 383800 383802 381326 383803 381327 381566 381567 381568 381569 381571 381572 381573 381574 381575 383017 383291 383292 383293 383294 383295 383296 383297 383298 383299 383300 383251 383254 383256 383257 383258 383260 383261 383262 383264 383266 383267 383268 383269 383690 383691 383692 383693 383026 383241 383244 383245 383247 383248 383249 3832 |
|---|
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-2959-2024%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.