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FDA: Panel Votes to Update Warning Labels On Yaz and Yasmin
Due to the influx of adverse events associated with drospirenone-containing contraceptives, officials from the U.S. Food and Drug Administration (FDA) convened on December 8 to discuss future regulations of newer birth control pills. According to a panel of outside experts, Yaz and Yasmin labels do not provide an adequate warning pertaining to the risk…
Fraudulent Stem Cell Practices Lead To FDA Warning
Stem cell research continues to be one of the most debated practices of the 21st century. While many suggest that such research is unethical, proponents profess that the benefits of stem cell research are limitless in their possibilities. While their nature remains ambiguous, stem cell therapies offer patients the potential to treat conditions that…
U-Prosta “Dietary Supplement” Recalled After FDA Discovers that the Product Includes Undisclosed Prescription Medication.
U-Prosta “Dietary Supplement” Recalled After FDA Discovers that the Product Includes Undisclosed Prescription Medication.. Read our informative blog to learn more about personal injury, defective products and sexual abuse cases.
Syracuse Scandal Increases Call For Reform of New York’s Statute of Limitations
An influx of sexual abuse scandals appear to be metastasizing across the country in a manner that has parents concerned for the well-being of their children. In the wake of the recent sexual abuse scandal that took place at Syracuse University, which witnessed the perpetrator avoid charges because of the statute of limitations, New…
Plavix® Thrombotic Thrombocytopenic Purpura Lawyer & Lawsuit
Thrombotic thrombocytopenic purpura (TTP) is a blood disorder that results in the abnormal creation of blood clots within several small vessels around the body. Subsequently, this condition is synonymous with potentially hazardous low platelet counts. While severe in nature, thrombotic thrombocytopenic purpura is relatively uncommon. However, the use of Plavix, a popular anti-platelet medication,…
CooperVision Avaira® Sphere Contact Lens Recall Lawsuit
CooperVision, in association with the U.S. Food and Drug Administration (FDA), was forced to conduct a nationwide Avaira Sphere contact lens recall on October 14, 2011. According to an official FDA Safety Notification, the recall was initiated after several lots of Avaira Sphere contact lenses were discovered to be harboring the unintended presence of…
Lap-Band Surgery Centers Accused of Insurance Fraud
Please note, The Senators (Ret.) Firm, LLP is no longer accepting Lap Band claims. If you feel that you may have a potential case, we urge you to locate another law firm adequately suited to handle your claim. Lap-Band surgery centers affiliated with the 1-800-GET-THIN advertising campaign have received a significant amount of criticism…
CooperVision Contact Lens Recall Lawsuit
CooperVision, a worldwide leader in the vision-care industry, has been the subject of recent controversy after several of their products were unintentionally adulterated during the developmental process. Avaira Toric and Avaira Sphere contact lenses, consisting of approximately five million units, have recently been recalled due to the unintended presence of silicone oil residue. According…