The Abiomed Impella® heart pump is a life-saving tool for patients suffering serious heart conditions. Being the smallest heart pump in the world, it was designed to assist with pumping when the heart is too weak to continue on its own. However, there has been an urgent recall on the device that has raised concerns about its safety from patients and healthcare providers. Why did this happen, and what steps should you take if you have been affected by the Abiomed Impella® heart pump recall? Our product liability attorneys provide more information.
The Abiomed Impella® heart pump is designed to temporarily support the heart when it cannot pump blood effectively. The device is commonly used in high-risk procedures, such as surgery for patients in heart failure, for elderly people, and for individuals suffering anterior infarction, better known as heart disease. The device functions by pumping blood and oxygen from the heart to the body. While the device has been known to be a lifesaver for many individuals, it has also caused some recent concerns.
In early 2024, over 66,000 of the Abiomed Impella® heart pumps were recalled due to reports of serious injuries and death. According to the FDA, there have been 129 serious injuries and 49 deaths reported so far. The devices have been associated with left ventricle perforation, free-wall rupture, hypertension, and reduced blood flow; all of which can lead to life-threatening complications or death. Patients who have undergone procedures using a recalled Impella pump should contact their health provider to discuss possible risks and outcomes.
The FDA has released that only certain models manufactured and distributed within a specific time frame have been affected by the recall. If your device was distributed between October 10, 2021 to 2023, your device may be recalled. The recall also included multiple models, such as the Impella 5.5 with SmartAssist.
If you or someone close to you has suffered complications due to a recalled Abiomed Impella® heart pump, you are not alone. The first step is to contact your healthcare provider in order to confirm whether or not your device was part of the affected line. Aside from seeking medical care, our experienced personal injury attorneys at Jan Dils can assist you through the process of seeking financial recovery.
Medical device manufacturers are responsible for ensuring their products are safe to use, and when they put patients in danger, they must be held accountable. As the largest female-founded law firm in the country, we are dedicated to fight for the financial recovery you deserve from any medical expenses, lost wages, and more.
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Jan Dils, Attorneys at Law
