Medical Devices Involved in Personal Injury Lawsuits
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America has the most expensive medical system in the world. Manufacturers justify this by claiming they are innovating, producing, and selling the most advanced medical devices in the world. What they don't say is that they often sell these expensive devices to patients without proper testing, and even after they discover the devices are actually causing injury.

Since 1955, we have been holding these medical device manufacturers accountable for the injuries they cause. Each year we help teach more than 1,500 attorneys how to successfully handle these types of cases.

Below is a sample of our current and previous litigation. Click on the below images and links to read extensive information on each topic.


Our Current Investigations and Lawsuits


Previous Investigations and Lawsuits

Alere InRatio

The use of the Alere INRatio and INRatio 2PT/INR Monitor System and INRatio Test Strips were associated with incorrect INR readings.

Bair Hugger

increased risk of joint infections linked to the use of this medical device during hip and knee replacement surgeries.

Depuy Hip

On August 24, 2010, DePuy Orthopedics issued a recall of the ASR XL Acetabular System and ASR Hip Resurfacing System, as they were failing at a higher rate than other types of hip replacements.


Hundreds of claims were filed against Bayer and Conceptus Inc. by women who suffered severe abdominal damage when their Essure birth control device moved and punctured the uterus and fallopian tubes.


In 2005 Guidant issued safety warnings on 11 models of defibrillators because of malfunctions with the magnetic switch inside the device getting stuck and preventing the device from providing treatment.


In 2005 Guidant issued safety warnings on 11 models of defibrillators because of malfunctions with the magnetic switch inside the device getting stuck and preventing the device from providing treatment.

IVC Filters

The lawsuits involving the IVC Filter alleged the manufacturers of the device failed to warn patients and physicians of the increased risks of the filter breaking, and metal fragments moving through the blood, potentially damaging an organ.


Nuvaring is a "third-generation" hormone contraceptive that has been associated with Stroke, Heart Attack, Deep Vein Thrombosis, Myocardial Infarction, Cerebrovascular Accidents, Pulmonary Embolism, Death.

Olympus Video Colonoscope

The Olympus Colonoscope can be difficult to properly clean after each use, which results in the device spreading a bacterial infection from one patient to another.

Ortho Evra

On November 10, 2005, Ortho McNeil, a division of Johnson & Johnson, warned millions of women using Ortho Evra that the birth control patch exposes them to significantly higher doses of hormones and may put them at greater risk for blood clots.

Penumbra Catheter

On December 15, 2020, the U.S. Food and Drug Administration (FDA) issued a warning letter regarding the urgent recall of the Jet7 Xtra Flex and Jet 7 MAX configuration devices, due to hundreds of recorded instances of these devices failing or causing injury.

Power Morcellators

Power Morcellators have been associated with an increased risk of significantly upstaging undiagnosed cancer during laparoscopic uterine fibroid removal surgeries.

Prisma Dialysis

The Prisma CRRT is a type of kidney dialysis system used in hospital intensive care units for critically ill patients. The FDA became aware of serious injuries and deaths associated with the use of the device in August 2005.

St. Jude Defibrillator

The St. Jude Implantable Cardioverter-Defibrillators and Cardiac Resynchronization Therapy Devices manufactured between 2010 and 2015 had issues with the battery prematurely failing without giving proper warning.

Stryker Hip

The Stryker hip recalls involve the LFIT Anatomic V40 femoral head utilized in the Stryker Accolade, and also the Rejuvenate and ABG II hip modules.

Surgical Stapler

Due to malfunctions, misuse, and defective design of surgical staplers, patients have suffered numerous types of injuries and complications, often with long-term or permanent consequences and/or requiring additional surgeries and treatments.

Transvaginal Mesh

In July 2011, the FDA issued heightened warnings regarding the use of transvaginal mesh for the repair of pelvic organ prolapse.

Zimmer Hip

In July 2008, Zimmer Holdings announced that it was suspending sales of the Durom acetabular cup, an artificial hip component, as a result of high implant failure rates.

Zimmer Knee

In September 2010, the FDA issued a recall on one particular Zimmer knee replacement product known as NexGen MIS.

Zimmer Shoulder

The Zimmer Biomet Comprehensive Reverse Shoulder System Humeral Tray Model 115340 manufactured between August 2008 and September 2011 was the subject of a recall.