Abiomed, Inc. recalls Impella LD intravascular micro axial blood pump, Product Number 005082
There is a potential risk for unintentional interaction of the Impella motor housing with the distal stent of a transcatheter aortic valve replacement (TAVR) resulting in destruction of the impeller blades. This has…
Read the official notice →- Date
- 2023-07-26
- Country
- United States
- Brand
- Abiomed
- Product
- Impella LD intravascular micro axial blood pump, Product Number 005082
- Classification
- Class I
- Units
- Worldwide distribution - US Nationwide.
- Category
- Drugs & medical
- Source
- FDA · Device
Copied automatically from the US Food and Drug Administration. Details may be shortened or out of date; the official notice is the authoritative source. Disclaimer
What to do
- Check the product name, strength and lot number against the official notice.
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- Ask the pharmacy or supplier about a replacement or refund.
General guidance from Recall Atlas. The official notice from the US Food and Drug Administration has the exact models, batch codes and remedy, and it takes priority.
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