Death & Injuries, Urgent FDA Recall on Heart Pumps
Serious Health Concerns Spark Major Recall
The FDA has issued an urgent recall for the HeartMate II and HeartMate 3 heart devices after they were linked to hundreds of injuries and at least 14 deaths. These devices, used to support patients with severe left ventricular heart failure, have been found to have significant risks associated with long-term use (KFF Health News) (HealthDay).
What’s the Issue?
The recall centers on the buildup of biological material in the devices, which can obstruct blood flow and impair the device's functionality. This obstruction typically occurs over two years or more, potentially leading to serious health risks, including death (American College of Cardiology).
Impacts and Responses
Despite the recall, the devices are not being removed from the market. Instead, Abbott Laboratories, the manufacturer, has communicated the risks to customers and is working with the FDA to address the issue. Physicians are advised to monitor patients for low-flow alarms, which indicate possible obstruction, and to take appropriate action such as stent implantation or device replacement (Pharma News Intelligence) (HealthDay).
Expert Opinions
Cardiologists like Sanket Dhruva from the University of California-San Francisco have emphasized the need for transparency and more thorough reporting of adverse events. Meanwhile, Francis Pagani, a cardiothoracic surgeon at the University of Michigan, highlighted the dilemma faced by patients reliant on these devices, noting that they remain the best available option despite their flaws (KFF Health News) (Pharma News Intelligence).
Moving Forward
The recall has prompted calls for improved communication between device manufacturers, healthcare providers, and regulatory bodies to ensure patient safety and timely reporting of device-related issues. As the healthcare community navigates these challenges, the focus remains on minimizing risks and enhancing patient care (American College of Cardiology) (HealthDay).
