Product Liability Lawyer Blog

November 19, 2013

Bayer Spends Billions on Yaz Settlements While Cases Still Pending

Bayer Pharmaceuticals has announced in the company’s stockholder newsletter that the company has spent almost $1.6 billion in settling cases arising from Yaz complications. Bayer manufactured both Yaz and Yasmin, two “fourth-generation” birth control pills that have been demonstrated to have serious unexpected side effects that Bayer failed to warn patients about. More than 10,000 women have filed lawsuits already, and despite the $1.6 billion settlement, estimates indicate that there are 9,873 claims still pending.

Bayer’s past settlements are good news for plaintiffs who wish to pursue claims against the drug company with the help of a Boston defective drug lawyer. Individuals who experienced harm as a result of Yaz or Yasmin can still come forward and take legal action against Bayer if they can prove that they were injured due to the use of these dangerous birth control products.
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November 13, 2013

Stryker Lawsuits Moving Forward as Defective Device Allegations Mount

by Jeffrey S. Glassman

Stryker hip replacement products continue to fail at high rates and cause serious complications for patients implanted with a hip replacement system that turned out to be much more dangerous than expected. Even as more patients continue to experience serious problems with Stryker products, cases are moving forward across the country with injured victims seeking to hold Stryker accountable for the damage the medical device company’s products have done.

The cases moving forward include claims that have been consolidated both into multi-county litigation and multi-district litigation. Our Boston Stryker hip lawyers know that many of these cases are proceeding on schedule and that plaintiffs may soon have the chance to be fully compensated for problems including metal toxicity, severe pain and failed hip replacements resulting in the need for revision surgery.
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November 11, 2013

Massachusetts Plaintiffs Seek Compensation for Defective Dialysis Products

by Jeffrey S. Glassman

Fresenius Medical Care is the largest provider of dialysis services in the United States. The company not only operates its own clinics but also manufactures equipment and dialysis drugs for others used throughout the United States. Because Fresenius produces drugs and medical products that are used in so many different clinics for patients undergoing dialysis, the company is required to ensure that its products are safe and the company must warn patients and physicians of any unexpected dangers, risks or side-effects that may occur due to product use.

Evidence indicates, however, that Fresenius failed to live up to this basic and important obligation. As a result, our Boston dialysis injury lawyers know that hundreds of dialysis patients experienced cardiac arrest, sudden heart attacks or death. Hundreds of cases have been filed already against Fresenius Medical Care and more than 312 of those cases are moving forward as part of a consolidated multi-district litigation in Massachusetts.
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November 9, 2013

Transvaginal Mesh Cases Move Forward After Ruling on Expert Witness

by Jeffrey S. Glassman

Thousands of transvaginal mesh lawsuits are moving forward within courts throughout the United States as injured women seek to hold manufacturers accountable for complications from dangerous surgical mesh products. In one case against transvaginal mesh manufacturer American Medical Systems (AMS), a recent judicial order was issued. The order addressed the request of plaintiffs to disqualify one of the witnesses that the defendant intends to present as an expert.

Our Boston transvaginal mesh lawyers know that mesh cases are heavily influenced by whose expert witnesses are most credible and by how convinced the jury is by the testimony of each expert witness. Mesh cases center on highly complex facts including whether the mesh product was the actual cause of harm when used as intended by the patient. Expert witnesses distill key facts for the jury, and having the right experts can make or break the case.
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November 7, 2013

Defective Airbags Lead to Vehicle Recall

by Jeffrey S. Glassman

Air bags are supposed to protect you in the event of an accident and if an air bag does not deploy when it is needed, serious or even fatal injury could result. At the same time, an air bag deploys at high speeds and if it deploys at the wrong time, it could cause a devastating accident. Because it is so important for air bags to work correctly, vehicle manufacturers must exercise care in the design and installation of air bags to ensure there are no problems.

Unfortunately, issues have arisen with air bags in certain Toyota vehicles including the 2012 and 2013 Toyota Camry, Camry Hybrid, Avalon, Avalon Hybrid and Venza vehicles. Our Boston defective products lawyers know that Toyota has recalled 885,000 vehicles worldwide as a result of potential air bag problems. An estimated 803,000 of the vehicles affected by the recall, including both crossovers and sedans, were sold in the United States. Drivers need to be sure to check if their vehicle is among the cars being recalled by Toyota so you can follow the manufacturer instructions and avoid injury from the dangerous vehicle defect.
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November 4, 2013

Massachusetts Appeals Court Reverses Dismissal of Pelvic Mesh Lawsuit

by Jeffrey S. Glassman

A plaintiff whose transvaginal mesh lawsuit was dismissed by the Suffolk County Superior Court has successfully won her appeal and her case will go forward. Our Boston transvaginal mesh lawyers know this is an important victory as the plaintiff will now get her day in court and will have a chance to demonstrate to a jury why she is deserving of compensation for her transvaginal mesh injuries.
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November 1, 2013

Americans Taking Advantage of Medical Devices, but the Risks Cannot be Understated

by Jeffrey S. Glassman

A surprising trend in recent years: middle-aged Americans are increasingly taking advantage of medical procedures that were typically reserved for the elderly. According to The Bulletin, “hundreds of thousands of [younger] Americans” are undergoing medical procedures to implant devices that can improve mobility.

Our Boston defective hip implant lawyers know that metal-on-metal hip implant products were largely marketed to younger consumers because they were supposed to provide advantages to the young and mobile. Unfortunately, these new metal hip replacements backfired when they turned out to be unreliable and dangerous. This means that as the medical device market shifts to accommodate increasingly younger patients, it is important that device manufacturers do everything possible to avoid future mistakes that lead to more defective products coming into the market.
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October 28, 2013

Toyota Settles Case After $3 Million Jury Verdict

by Jeffrey S. Glassman

In 2010, Toyota vehicles began accelerating unintentionally, causing the company to stop production and sales of eight vehicle models and to recall 2.3 million vehicles. Toyota’s reputation was damaged and the company has been subject to many lawsuits both from plaintiffs who were injured or who lost family members, and from plaintiffs who experienced a decline in the resale value of the vehicles.

Our Boston defective products lawyers know that Toyota can be held responsible if it is found that their products were dangerous when used as intended and caused harm to plaintiffs. Now, Toyota has suffered the first loss in court in an unintended acceleration case, which prompted Toyota to then settle several claims after the jury awarded $3 million to a plaintiff in an unattended acceleration case.
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October 25, 2013

Stryker Hip Recall Litigation Could Cost More Than $1 Billion

by Jeffrey S. Glassman

Stryker Corp. recalled its ABG II and its Rejuvenate hip implants from the market last year because the products were causing serious harm to patients. Our Boston defective hip implant lawyers know that in the United States, as many as 20,000 of these Stryker devices have already been implanted in patients. The recall comes too late to protect these patients from complications. But fortunately these patients will get financial help and future harm will be prevented since these dangerous medical devices have now been taken off of the market.

The recall is also expected to result in a massive cost to Stryker, which may be why the recall took so long for the company to order even once it became apparent that its hip replacement products were not working as promised.
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October 21, 2013

A New Approach to Hip Replacement Surgery

by Jeffrey S. Glassman

Defective hip replacements have caused a significant number of problems for patients, requiring follow-up surgeries and medical care. Despite the risk of defective hip-replacements thousands of Americans undergo the surgery every year to improve their quality of life. Patients who have endured the surgery know that it is extremely invasive and can involve months of recovery. Now an alternative approach to hip replacement could reduce recovery time and provide a better treatment solution for patients.

Many patients with arthritis and other hip problems will seek out hip replacement therapy. While some hip implants have changed the lives of patients, others have caused additional complications and injuries. Our Massachusetts defective medical device attorneys are dedicated to helping victim of defective hip implants pursue recovery from negligent manufacturers. We are also aware of the risk of hip replacement surgery and the benefit that it provides to many patients.
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