Abiomed and Johnson & Johnson Prioritized Profits Over Patient Safety – Victims and Their Families Deserve Justice
Have you or a loved one suffered a severe injury, or did a loved one pass away, because of an Abiomed Impella heart pump? You may be entitled to compensation.
The FDA has issued the most serious CLASS 1 RECALL for these Impella devices, warning that they pose a risk of "serious adverse health consequences, including left ventricle perforation or free wall rupture, hypertension, lack of blood flow, and death."
"These companies put profits before people, and now they must face the consequences."
OR CALL 1-800-709-0014
Despite knowing about these deadly risks for years, Abiomed and J&J concealed this information and continued to profit off of these dangerous products. In fact, Abiomed first raised the warning about issues with the Impella devices in October 2021, but failed to report the serious adverse events and deaths to the FDA in a timely manner.
It wasn't until late December 2023 that Abiomed finally sent an urgent correction letter to customers warning of the dangers and urging caution. By that time, the damage had already been done, with over 300,000 of these Impella devices used in patients worldwide.
The defective medical device compensation experts at Danziger & De Llano law firm are committed to holding Abiomed and Johnson & Johnson accountable for their reckless actions.
"Patients put their trust in these medical devices, only to have it betrayed by companies that cared more about profits than their well-being. We won't stop until Abiomed and Johnson & Johnson are held accountable for all the harm they've caused."
If you or a loved one suffered a heart attack, arrhythmia, or death after being implanted with an Abiomed Impella heart pump between 2021 and 2024, you have the right to seek justice and compensation.
OR CALL 1-800-709-0014
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