Explore lawsuits involving medical devices.
Medical device lawsuits involve claims related to implanted devices, surgical products, recalled devices, revision surgeries, complications, or alleged product defects.
Educational information only. Not medical or legal advice. No attorney-client relationship is formed. Do not make medical decisions based on this website.
Where these claims most often arise.
Medical device claims may involve implanted devices, surgical mesh, joint replacements, cardiac devices, filters, pumps, monitors, surgical tools, or other products used in medical care.
These cases are often connected to broader product liability principles because the device may be evaluated as a product with design, manufacturing, labeling, warning, and safety-related issues.
- Implants
- Hernia mesh, joint replacements, cardiac stents, IVC filters
- Devices
- Pumps, monitors, surgical tools, diagnostic equipment
- Common issues
- Defect, failure, recall, revision surgery, infection
What these lawsuits often allege.
Medical device lawsuits may involve several types of allegations depending on the device, injury, warning history, recall status, medical records, and state law.
Design defect
Allegations that the device was unsafe because of how it was designed.
Manufacturing defect
Allegations that the device was improperly made or contaminated.
Failure to warn
Allegations that warnings, instructions, or risk information were inadequate.
Device failure
Allegations that a device fractured, migrated, degraded, loosened, or failed to work as expected.
Recall-related issues
Allegations involving safety communications, recalls, withdrawals, or known device problems.
Revision surgery
Claims involving additional procedures required after device complications, removal, or replacement.
These are general categories. A case review request does not mean that a device was defective or that a legal claim exists.
Information that may help.
A reviewing firm may look for information that helps identify the device, timing, complication, medical history, and possible connection between the device and the alleged harm.
- The device name, manufacturer, model, serial number, or implant card information
- Date of implantation, surgery, removal, revision surgery, or complication
- Medical records, operative reports, imaging, pathology reports, or device records
- Symptoms, diagnosis, complications, infections, device failure, or additional surgeries
- Whether the device was recalled or identified in warnings or safety communications
- Whether the device was preserved, photographed, removed, replaced, or documented
Medical device claims can be highly fact-specific and often require careful review of medical records, product identification, timing, warnings, and state law.
This is not medical advice.
Do not stop treatment, delay care, remove a device, or make medical decisions based on information from this website. Speak with a qualified healthcare provider about symptoms, complications, treatment options, or device concerns.
Lawsuit Center does not diagnose conditions, evaluate medical causation, or determine whether a device caused a particular injury.
Considering a medical device case review?
If you believe a medical device may be connected to a serious injury, complication, revision surgery, infection, device failure, or other harm, you can explore whether case review fits.
A case review request does not guarantee eligibility, compensation, contact from a law firm, or legal representation.