Legal Investigation into Inspire Sleep Apnea Implant Injuries

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Inspire Sleep Apnea Implants Under Investigation for Shocks, Malfunctions, and FDA Recall

Inspire Sleep Apnea Implants Recalled for Electrical Shocks and Malfunctions

If you have an Inspire sleep apnea implant and experienced painful electrical shocks, inconsistent stimulation, or needed a revision surgery, you may not be alone. The product liability attorneys at mctlaw are currently investigating legal claims involving the Inspire Implantable Pulse Generator (IPG), including but not limited to models under an FDA recall.

In June 2024, the FDA issued a Class 1 recall, its most serious type, for two Inspire IPG models: 3028 and 3024. The recall warns that the devices may cause electrical leakage or deliver painful shocks due to a manufacturing defect. But reports from patients suggest that problems may go beyond the recalled models.

Why We’re Investigating Inspire Implants

Many patients have reported serious complications with their Inspire devices, including unexpected electrical shocks even when the device is turned off. In many cases, people say their concerns were dismissed by healthcare providers or device representatives. Our goal is to make sure these experiences are documented and evaluated.

Some patients describe these types of unusual complications with their Inspire implants:

• Unexpected shocks to the tongue or throat
• A complete stop in therapy due to battery failure
• Frustration after doctors or company reps said the device was “working normally”

Even if your Inspire model was not recalled, we want to hear from you. Our attorneys are investigating cases involving Inspire implant electrical stimulation problems or device failures.

Inspire Sleep Apnea Implant Investigation: What You Need to Know

We want to be upfront: this is an ongoing investigation. Based on the product recall and reports from patients, we believe there is enough concern to take a closer look.

We may take you on as a client to investigate these issues more thoroughly. This includes reviewing your medical records and any documentation related to your Inspire device and symptoms.

However, it is important to understand that during this process, we may determine that your situation does not match the specific type of legal claims our firm is focused on pursuing.

This investigation is still in the early stages. There is no guarantee that your case, or any case, will move forward or result in compensation. Whether we continue with legal action depends on what we find during our initial review of your situation.

Do You Qualify for an Inspire Case Investigation?

We are currently reviewing cases involving the Inspire IPG under the following conditions:

• You are experiencing electrical shocks or jolts from the device while it is turned off.
• Your Inspire IPG has been removed or revised due to complications or because of the product recall.
• Your healthcare provider or Inspire representative dismissed your concerns about shocking or device malfunction.
• You have revision surgery scheduled, or your doctor has recommended removal of the device due to issues with unintended electrical stimulation.

You do not need to have one of the officially recalled models to be considered. We are reviewing all reports of abnormal electrical behavior or other dangerous device issues.

What Happens Next?

If you contact us, there is no obligation to file a claim. Speaking with our team is simply the first step in helping us understand what is happening to patients. Your experience could be key in determining whether this situation leads to broader legal action.

The attorneys at mctlaw have decades of experience handling defective medical device cases across the country. If you are dealing with unusual sensations, shocks, or other problems related to your Inspire implant, we want to hear from you.

There is no obligation or pressure to speak with our legal team. We are working directly with people who had issues with their Inspire IPG. You do not need to wait for another FDA warning to take action.

Let us know if you’re experiencing shocking sensations or any unusual changes in how your Inspire implant works. We want to hear your story. The product liability attorneys at mctlaw have a long track record of successfully representing people injured by defective medical devices across the United States.

Attorneys Jessica Olins, Altom Maglio, and Michael Cowgill are leading this investigation. We are here to help you understand your options.

What Is the Inspire Sleep Apnea Implant?

Doctors surgically implant this device to treat obstructive sleep apnea (OSA), a condition that causes repeated breathing interruptions during sleep. OSA happens when soft tissue in the throat collapses, partially blocking the airway with the tongue.

The Inspire implant sends electrical pulses to airway muscles, moving the tongue out of the way so users can breathe. Doctors place the device near the collarbone during surgery. This treatment is meant for patients who haven’t had success with CPAP machines.

Content Reviewed by Altom Maglio – Attorney

Altom M. Maglio represents individuals across the United States in complex civil litigation, including COVID eviction moratorium takings claims, rails to trails conversions, listeria outbreak lawsuits, defective orthopedic devices and product liability lawsuits. Mr. Maglio founded mctlaw in 1999 to represent people in their fight against huge corporations and large government programs. He is also an active leader in the U.S. Court of Federal Claims Bar Association and the American Association for Justice Leadership Forum.

Altom Maglio Attorney Bio

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