Medical devices often play a crucial role in diagnosing and treating serious medical conditions. However, patients who use defective or dangerous medical devices may end up in a less desirable position than they started. Companies whose products cause harm to patients may be liable under Maryland’s product liability laws. While a defective product lawsuit may not make a person whole again or undo the harm they experienced, it can relieve some financial burdens.
The Food and Drug Administration (FDA) recently issued a recall statement alerting those who use specific Philips ventilators, CPAP, and BiPAP machines. The recall follows a June 2021 safety report that advised healthcare providers and consumers that these devices may pose potential health risks. The FDA’s investigation in conjunction with the company’s testing revealed that foam degradation in the product is toxic and might emit carcinogens. Philips explained that the foam might release toxic fumes and particles that users may swallow or inhale. While the company stated that they were replacing and repairing the machines, the process may take upwards of a year. Further testing also showed that the replacement foam poses many of the same risks as the original product.
Many users have reported injuries related to defective machines, such as:
- Bladder Cancer
- Brain Cancer
- Breast Cancer
- Kidney Cancer
- Respiratory Distress System
- Heart Failure and Attack
- Liver Cancer, Damage, and DIsease
- Lung Cancer, Damage, and Disease
These injuries can have lifelong consequences on the user and their loved ones. In addition to these conditions come users reported side effects such as: