Which NuVasive & Precice Devices Have Been Recalled?
NuVasive has recalled several stainless steel and titanium-based Precice devices due to potential injury risks they present to patients.
Stainless Steel-Based NuVasive Products
While the company hasn’t confirmed the exact cause of the stainless steel product defects, reports seem to indicate problems where the telescoping (moving) parts of nails come together. There may also be issues regarding wear, corrosion, and exposure of various components.
Recalled stainless steel-based (Biodur 108) Precise devices include:
Since personal injury cases are widely diverse, there is no one-size-fits-all answer to what a personal injury settlement could mean for you and your family — call Osborne & Francis at (561) 293-2600 to have your specific questions answered.
- Precice Bone Transport
- Precice Plate
- Precice Stryde
Patients with stainless steel NuVasive Precice devices are currently reporting pain and changes in bone and soft tissue surrounding the implants. You should contact a lawyer if you have been fitted with a stainless steel Precice device and are experiencing any pain or changes in the area.
Titanium-Based NuVasive Products
The FDA has not yet received reports of biocompatibility connected with titanium-based Precice implants. Nevertheless, NuVasive is currently investigating various titanium-based products for similar adverse events detected with the stainless steel products.
Recalled titanium-based Precice devices include:
While no lawsuit can fully undo an injury and what you’ve been through, the damages award can provide financial assistance for:
- Precice Freedom
- Precice Intramedullary Limb Lengthening (IMLL) Device
- Precice Short
- Precice Unyte
In general, titanium-based implants are associated with various disadvantages, including low biologic activity. This can in turn reduce growth of fibrous tissue, allowing for loosening of the implant, inflammation, abrasion, and other allergic reactions.
Thus, whether you or a loved one were fitted with stainless-steel or titanium Precice devices, you may need to contact a lawyer to determine the status of the product. Even if your product is not on the recall list, it could be subject to recall or investigation in the future.
What Do Damages Awards From NuVasive Precice System Lawsuits Cover?
While each case may be different, damages awards from a NuVasive Precice System lawsuit can cover a wide range of costs and expenses, including:
- Medical and hospital bills
- Costs of additional corrective surgery (known as “revision surgery”)
- Expenses not covered by traditional insurance
- Lost wages and loss of the ability to generate income
- Pain and suffering
- Loss of companionship of a loved one
Damages will vary depending on various factors, including the severity of the injuries involved, the extent of the lifestyle changes, and even the skill or experience of the attorney handling the case. This is why it’s important to contact a lawyer with a proven background in medical device litigation.
If you are unsure of whether you qualify to file a lawsuit, contact the lawyers at Osborne & Francis at (561) 293-2600 for more guidance and direction. Investigations are still ongoing, and new information may shed new light on potentially affected products.
What Injuries Were Named in This Lawsuit?
NuVasive Precice System lawsuits are focusing on biocompatibility injuries — complications caused by the body reacting poorly to the implant device. These include bone problems, tissue reactions, and other injuries.
In particular, patients with Precice Stryde implants had pain and abnormal growth at the nail junction. Retrieved nails were found with corrosion and discoloration, and biological material was found in the nail.
NuVasive is currently investigating health problems linked to biocompatibility issues with its Precice devices, including:
- Cancer
- Chronic toxicity
- Developmental toxicity
- Reproductive toxicity
These types of injuries are often caused by improper or incomplete testing for biocompatibility. In such cases, the manufacturer responsible for such defective products must be held liable for their misconduct.
Seek immediate medical attention and contact a lawyer if you believe you may have been injured by NuVasive Precice products.
How Do I Qualify to Join This Lawsuit?
Patients with the following conditions may qualify for a NuVasive Precice System lawsuit:
- Bone abnormalities
- Bone degradation
- Cancer
- Developmental Effects
- Pain
- Reproductive System Problems
- Skin Irritation or Burns
- Tissue Death (necrosis) Around the Implant
- Thrombosis
- Tissue Degradation
Additional eligibility factors may include:
- You had a Precice device implanted onto your limb or your spine
- You were at 18 years old or older at the time of the implant
- Your device was implanted in or after the year 2013
- Your device was adjusted using magnetic mechanisms or the remote external control
If you are unsure of whether you qualify to file a lawsuit, contact the lawyers at Osborne & Francis at (561) 293-2600 for more guidance and direction. Investigations are still ongoing, and new information may shed new light on potentially affected products. As mentioned, filing deadlines apply, so don’t delay in reaching out for assistance.