Reasons to Consider Legal Action for a Defective Device
Legal action can secure compensation for medical expenses, rehabilitation, lost income, and ongoing care related to device injuries. It can also address non-economic losses such as pain and diminished quality of life.
Pursuing a claim can promote accountability, leading to product fixes, recalls, or improved warnings that protect others from similar harm. For many clients, the combination of recovery and accountability is an important outcome.
Common Situations Where Claims Arise
Claims often stem from device failures during or after surgery, implant breaks or migrations, contamination of devices, mislabelling or missing instructions, and inadequate warnings about known risks.
Implant Failure or Migration
Devices such as joint replacements, cardiac implants, or mesh that break, move from their intended position, or wear prematurely can cause significant injury and typically require revision surgeries or long-term treatment.
Manufacturing Contamination or Defects
Contamination during manufacturing or assembly defects can lead to infections, device malfunction, or early device failure. Tracking production records and complaint histories can reveal patterns of defective manufacture.
Lack of Adequate Warnings or Instructions
When manufacturers fail to disclose known risks or provide clear instructions for safe use, patients and clinicians may be unaware of hazards that could have been mitigated with proper labeling and training.