Hernia Mesh Injury

Injured by a Hernia Mesh?

If a documented device failure caused serious injury, you may be entitled to compensation.

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A case specialist will follow up within two business days.
Strict filing deadlines may apply; do not wait.

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Examples

Injuries Involving Medical Devices.

This list is not exhaustive. Whether your device is listed below or not, you may still have a valid legal claim. The strength of any claim depends on the specific facts and circumstances of your case. Past results in similar cases do not guarantee a similar outcome in yours.

Manufacturers and distributors of medical devices have a legal duty to ensure their products are safe and properly labeled. When they fail, patients can suffer serious, life-altering harm.

Hip & Knee Implants

Metal-on-metal hip implants and certain knee replacement systems have been linked to metallosis, premature loosening, fracture, and the release of metallic debris into surrounding tissue — often requiring painful revision surgery.

Hernia Mesh

Certain hernia mesh products have been recalled or linked to serious complications including infection, adhesion to organs, mesh migration, and bowel obstruction — often requiring additional surgeries to correct.

Transvaginal Mesh

Pelvic mesh implants used to treat stress urinary incontinence or pelvic organ prolapse have caused severe complications, including mesh erosion through vaginal tissue, chronic pain, and organ perforation.

IVC Filters

Retrievable inferior vena cava filters designed to prevent pulmonary embolism have fractured and migrated in some patients, with filter fragments traveling to the heart or lungs, causing life-threatening complications.

Spinal Cord Stimulators

Malfunctions including lead migration, electrical shorts, and device failure have caused serious injuries in patients relying on spinal cord stimulators for chronic pain management, sometimes requiring surgical explantation.

Defibrillators & Pacemakers

Lead fractures, battery failures, and software defects in implantable cardiac devices have been associated with inappropriate shocks, failure to pace, and in severe cases, cardiac events requiring emergency intervention.

Breast Implants

Certain textured breast implants have been linked to breast implant-associated anaplastic large cell lymphoma (BIA-ALCL), a rare but serious immune system cancer. Allergan's BIOCELL implants were recalled by the FDA in 2019.

Other Recalled Devices

If you were seriously injured by any other FDA-recalled or defective medical device, you may still qualify. Tell us what device you used and what happened — we evaluate each case individually.

How It Works

What happens after you submit.

No upfront cost. No obligation. Free review of whether your situation fits the criteria.

Submit Your Information

Answer a short set of questions — under 2 minutes. Your information is kept confidential.

Talk to a Case Specialist

A specialist will reach out within two business days to learn more about your situation and answer your questions.

Review Your Options

If your case qualifies, we connect you with an experienced attorney. No fee unless we recover.