Medical devices are designed to save lives, improve health, and restore mobility. From heart pacemakers and surgical implants to hospital equipment and diagnostic tools, patients trust that these products are safe, thoroughly tested, and effective. Unfortunately, that trust is sometimes misplaced.
When medical devices are defectively designed, poorly manufactured, or improperly marketed, the consequences can be devastating. Patients may suffer severe injuries, permanent disability, or even death — often after undergoing invasive procedures they believed would help them heal.
At Moore Payne Law, Attorneys Geoff Moore and Spencer Payne represent patients across Florida who have been seriously harmed by defective medical devices and equipment. Their mission is to hold manufacturers and other responsible parties accountable and to help victims recover the compensation they need to rebuild their lives.
What Is a Medical Device Failure?
A medical device failure occurs when a product used for diagnosis, treatment, or surgery does not perform as intended and causes injury to a patient. These failures may result from flaws in design, errors during manufacturing, or inadequate warnings about known risks.
Unlike simple consumer products, medical devices are often implanted inside the body or used during critical medical procedures. When they fail, removal or correction may require additional surgery, prolonged recovery, or lifelong medical care.
Common Types of Defective Medical Devices
Defective medical device claims can involve a wide range of products, including:
- Hip and knee replacement implants
- Surgical mesh used for hernia or pelvic repair
- Pacemakers and defibrillators
- Insulin pumps and infusion devices
- Artificial heart valves
- Spinal implants and fixation devices
- Catheters and stents
- Diagnostic and monitoring equipment
In many cases, manufacturers were aware of potential defects but failed to address them before releasing products to the market.
How Medical Device Defects Occur
Medical device failures often stem from preventable corporate decisions. Common causes include:
Design Defects
The product is inherently unsafe due to poor design, even when manufactured correctly. For example, an implant may wear down too quickly or interact dangerously with surrounding tissue.
Manufacturing Defects
Errors during production, contamination, or use of substandard materials may cause individual devices to fail.
Failure to Warn
Manufacturers may fail to provide adequate instructions or warnings about known risks, side effects, or complications.
Inadequate Testing
Some devices are rushed to market without sufficient clinical trials or long-term safety studies.
When profits are prioritized over patient safety, the results can be catastrophic.
Injuries Caused by Defective Medical Devices
Medical device failures can lead to serious and sometimes irreversible injuries, including:
- Chronic pain and inflammation
- Infection or sepsis
- Nerve damage
- Internal bleeding or organ damage
- Implant loosening or migration
- Device breakage inside the body
- Loss of mobility or function
- Need for revision or removal surgery
In the most severe cases, defective devices can cause fatal complications.
Who Can Be Held Liable in Medical Device Injury Cases
Medical device injury claims often involve multiple responsible parties. Depending on the facts, liability may extend to:
- Medical device manufacturers
- Component part manufacturers
- Distributors and suppliers
- Testing laboratories
- Sales and marketing companies
- Hospitals or healthcare facilities (in certain cases)
Under Florida product liability law, manufacturers may be held strictly liable, meaning victims do not always need to prove negligence — only that the device was defective and caused harm.
Medical Device Recalls and Patient Rights
Many defective medical devices are eventually recalled after injuries are reported. However, a recall does not automatically compensate injured patients.
Patients may still have legal rights even if:
- The device has been recalled
- The recall occurred after implantation
- The manufacturer claims the device was FDA-approved
FDA approval does not shield manufacturers from liability when products are defective or unreasonably dangerous.
Moore Payne Law helps patients understand how recalls impact their legal options.
Proving a Medical Device Injury Claim
Medical device cases are complex and require extensive investigation. To succeed, it must generally be shown that:
- 1.
- The medical device was defective or unreasonably dangerous
- 2.
- The defect existed when the device left the manufacturer’s control
- 3.
- The device was used as intended or in a foreseeable way
- 4.
- The defect directly caused the patient’s injury
Moore Payne Law works with engineers, medical experts, and product specialists to analyze device failures and build strong, evidence-based cases.
Compensation Available to Victims
Patients injured by defective medical devices in Florida may be entitled to compensation for:
- Medical bills and hospital expenses
- Corrective or revision surgeries
- Rehabilitation and physical therapy
- Long-term medical care
- Lost wages and reduced earning capacity
- Pain and suffering
- Emotional distress
- Permanent disability or disfigurement
In fatal cases, surviving families may pursue wrongful death compensation.
Challenges in Medical Device Litigation
Medical device manufacturers are often large corporations with significant legal resources. They may attempt to:
- Deny the existence of defects
- Blame doctors or patients for complications
- Argue FDA compliance as a defense
- Delay proceedings to pressure settlements
Experienced legal representation is critical to overcoming these tactics.
How Moore Payne Law Handles Medical Device Cases
Attorneys Geoff Moore and Spencer Payne take a meticulous, trial-ready approach to medical device litigation, including:
- Reviewing device design and testing records
- Investigating prior complaints and recalls
- Consulting medical and engineering experts
- Analyzing regulatory compliance
- Negotiating aggressively with manufacturers and insurers
- Preparing cases for trial when necessary
Their commitment ensures that powerful corporations are held accountable for patient harm.
What Patients Should Do After a Device Failure
If you suspect a medical device caused injury:
- 1.
- Seek immediate medical attention
- 2.
- Preserve the device if it is removed
- 3.
- Request copies of medical records
- 4.
- Document symptoms and complications
- 5.
- Avoid speaking with manufacturer representatives
- 6.
- Contact Moore Payne Law for legal guidance
Early action helps protect evidence and strengthens your claim.
Standing Up for Injured Patients Across Florida
Medical devices are meant to heal — not harm. When defective implants or equipment cause serious injuries, accountability is essential to protect both victims and future patients.
Moore Payne Law is committed to standing up for Floridians harmed by unsafe medical devices. Attorneys Geoff Moore and Spencer Payne combine experience, compassion, and relentless advocacy to pursue justice and meaningful compensation.
If you or a loved one has been injured by a defective medical device in Florida, contact Moore Payne Law today for a free and confidential consultation. The right legal team can make all the difference in your recovery and future.
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