Posted On: February 25, 2008

Thousands Die Over Delay By Bayer To Recall Bayer AG Drug

Some 22,000 people's lives were needlessly snuffed out because of Bayer's colossal failure to recall its Bayer Ag drug, Trasylol, that is used during surgery to stop and control bleeding during open heart surgery. In the fall of last year, the drug was withdrawn after the FDA requested Bayer to do so after finding out from a study that connected the medicine to organ failure requiring dialysis.

Numerous Plaintiffs have filed wrongful death lawsuits against Bayer for injuries sustained while on the defective drug and more are expected.

If you or a loved one has been affected by this or any other defective drug, I would invite you to visit my website, www.samlevine.com or contact my office, Sam Levine, Attorney at Law.


Posted On: February 12, 2008

FDA Warns That Baxter's Heparin Should Not Be Used

The FDA just warned consumers and the health care community that Heparin, made by Baxter Health Care, should not be used. Heparin has been linked to numerous illnesses and the deaths of at least a handful of people.

Before FDA issued this warning, Baxter asserted that it would stop making the defective medicine after it was reported that people were experiencing allergic reactions, which occurred within minutes after ingestion and included rapid heartbeat, nausea and swelling.

If you or a loved one has been adversely affected by this or any other defective or recalled medicine, I would invite you to visit my website, www.samlevine.com or contact my office, Sam Levine, Attorney at Law.


Posted On: February 2, 2008

Deadly Cordis Balloon Catheters Recalled by Johnson & Johnson

In the wake of injuries to two people, Johnson & Johnson has recalled defective balloon catheters utilized by surgeons during angioplasties. The injuries occurred because the balloons did not deflate as they should have and therefore, they have been recalled as a Class 1 Recall, which is the highest level of recall. What this means is that there is a fair likelihood that use of this defective medical device could lead to serious complications, like injury or death.

The real danger of the defective Cordis Balloon Catheters is that they have a tendency to slowly deflate when they are inserted into an artery during the angioplasty procedure. The obvious complication is that the use of this defective medical device this could lead to a partial or total blockage of the artery causing a heart attack.

In mid January 2008, Johnson & Johnson sent customers in the United States a letter about the recall with a directive to consult with their respective doctors.

If you or a loved one has been injured by this or any other defective product, I would invite you to visit my website, www.samlevine.com or contact my office, Sam Levine, Attorney at Law.

Posted On: February 1, 2008

Pain Caused By Defective Mentor ObTape Vaginal Sling Leads to Lawsuits

As you may recall, a series of lawsuits related to injuries caused by defectively designed ObTape Vaginal Slings were filed by numerous women in the Atlanta, Georgia area back in November of 2007. The defective medical device is made by Mentor, Inc. and was designed and marketed to help women manage incontinence and maintain bladder control. This defective medical device has caused numerous women a multitude of problems and complications, which has led to a flurry of lawsuits across the county as recently as late January 2008.

As a direct result of the use of the Mentor ObTape Vaginal Sling, women are suffering from erosions of the vaginal wall and the urethra. This is causing women severe pain and is necessitating women have to have multiple surgeries to treat these conditions. Another complication that women are experiencing is that the device is cutting into the vaginal wall.

In the lawsuits, in addition to the Plaintiff's alleging that the Vaginal Sling is defectively designed, it is also alleged that the mesh on the sling came apart and that parts of the mesh material that make up the sling became embedded in the vaginal wall, causing women to experience pain, infections and bloody discharges, among other things. These women are now faced with having to have the defective vaginal sling surgically removed, which is by all accounts, considered a complex and lengthy procedure.

Women across the Atlanta, Georgia area and the rest of the county were hoping that the vaginal sling made by Mentor, Inc. would help them with their bladder and incontinence issues, but instead the mere presence of this defective medical device has lead to a plethora of medical problems and in turn to serious litigation.

If you or a loved one has been affected by this or any other defective medical device, I would invite you to visit my website, www.samlevine.com or contact my office, Sam Levine, Attorney at Law.