On October 27, 2023, the US Food and Drug Administration (FDA) has designated a Class I recall, its highest severity classification, on the Philips Respironics V60 and V60 Plus Ventilators. This is a matter of utmost concern, as the usage of these medical devices could lead to severe injuries or fatalities. This recall signifies a voluntary correction taken by Philips Respironics rather than the complete removal of the product from the market.
The specific devices under this recall are the Philips Respironics V60 and V60 Plus Ventilators. These ventilators, primarily used within hospitals, serve the critical function of aiding pediatric and adult patients with their breathing by supplying a fixed percentage of oxygen.
Why Are the Devices Being Recalled?
The recall was initiated after it was discovered that the Power Management Printed Circuit Board Assemblies (Power Management PCBA) within these ventilators, supplied by a third-party warehouse, failed to meet the stipulated standards for ventilators. A significant concern is that these ventilators are sometimes utilized outside of Intensive Care Units (ICUs), where patients might not be under direct surveillance. This could pose an increased risk, especially in settings where patients aren’t continually monitored. The faulty components in the ventilators might lead to dangerous health consequences, including death. To date, there haven’t been any reported injuries or deaths linked to this issue.
Individuals most at risk include patients relying on these ventilators for breathing support and healthcare professionals tending to these patients. As an immediate corrective action, Philips Respironics sent out an “Urgent Medical Device Correction” letter to all affected customers on August 25, 2023, advising them to halt the use of these devices and set them aside. Philips Respironics representatives will then reach out to these customers to guide them on either removing or replacing the Power Management PCBAs in the affected units.
For those seeking additional details or assistance regarding this matter they can contact their regional Philips Respironics representative or reach out to the Philips Respironics Customer Care Solutions Center directly.
Possible Recourse for Affected Individuals
In situations where medical devices have the potential to cause harm, victims might have the legal right to seek compensation through a product liability lawsuit. If an individual has suffered harm or injury due to the use of the recalled Philips Respironics V60 or V60 Plus Ventilators, they might be eligible to file a lawsuit to recover damages. These damages can include compensation for medical expenses, pain and suffering, lost wages, and other related costs.
The process begins by gathering evidence, including medical records, proof of device usage, and any documentation of adverse effects experienced. Expert testimony, particularly from medical professionals, can further bolster a claim, elucidating how the faulty device directly caused harm to the patient.
Take Action with Parker Waichman LLP
For those affected by this recall and seeking legal advice or representation, Parker Waichman LLP, a renowned national product injury law firm, is offering a free consultation. By dialing 1-800-YOUR-LAWYER (1-800-968-7529), victims can directly connect with experienced attorneys who can provide guidance on potential legal recourse and compensation. Don’t wait; take the necessary steps to protect your rights today. Regardless of your location or where your injury occurred, our nationwide personal injury law firm is ready to assist you.
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