[Recalled] Impella 5.5 SmartAssist S2 Set, JP; Product Code: 1000459; — A potential device interaction between the Shockwave Coronary IVL Catheter and… | FDA 2024-08-05
The product on this page is subject to an official recall. We summarise the regulator's findings and the recommended action.
Recall details
| Product | Impella 5.5 SmartAssist S2 Set, JP; Product Code: 1000459; |
|---|---|
| Brand / manufacturer | Abiomed, Inc. |
| Category | device |
| Issuing authority | FDA_DEVICE |
| Reference | Z-2970-2024 |
| Country of notice | United States |
| Risk level | Class II |
| Hazard type | recall |
| Notice date | 05 August 2024 |
| EAN / barcode | 00813502013054 |
Why it was recalled
According to the FDA_DEVICE notice, the identified hazard is: 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.
This Class II recall concerns device products distributed in United States and was recorded by FDA_DEVICE. Recalls in this category are published so that owners, retailers, and importers can identify affected units and act quickly.
What to do if you own this product
Check whether your unit is affected and follow the authority's guidance before further use.
Read the full official notice →
Related recalls from Abiomed, Inc.
This page indexes a public government recall notice for reference. We do not sell or verify this product; always confirm the current status on the authority's official site.