Tag Archives: Medical Device Guardian’s Act
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Pradaxa not Fit for a Dog, Family of Alleged Pradaxa Bleeding Victim Claims
The family of a Texas woman who died just months before her 60th wedding anniversary believes she would be alive today were it not for Pradaxa (dabigatran). According to a report from the Houston Press, Pradaxa patient Loraine Franklin fell and hit her head last December, resulting in an intracranial ...
Actos, Avandia May Up Risk for Diabetic Macular Edema
A newly published study is raising concerns that patients who take Actos or Avandia may face an increased risk of developing diabetic macular edema, an eye disorder that can result in vision loss. The study, published in the Archives of Internal Medicine, found that type 2 diabetics who use thiazolidinediones, ...
Pennsylvania Health System Proposes Comprehensive Fracking Study
A proposed study would examine the health effects of hydraulic fracturing (fracking) drilling on the people living closest to active natural gas wells.
Study Suggests Hormonal Contraceptives Linked to Increased Brain Tumor Risk
A study of Danish women of reproductive age suggests that long-term use of hormonal contraceptives is associated with an increased risk of brain tumors.
Major Retailers Accused of Selling Fraudulent Herbal Supplements
The NYS attorney general’s office has accused four national retailers of selling fraudulent dietary supplements.
Three Injured When Long Island Railroad Train Hits Car on Tracks
Three people, including a train engineer, were injured on Wednesday when a Long Island Rail Road train hit a livery cab on the tracks west of Wyandanch station, LIRR officials said. LIRR spokesman Salvatore Arena said the driver of the Lincoln Town Car was taken to Good Samaritan Hospital Medical Center ...
Smith & Nephew Recalls Metal-on-Metal Hip Implant Component
Medical device maker, Smith & Nephew, just issued a recall for a metal-on-metal hip implant component, a part of one of its all-metal hip replacement systems.
What Action Will the FDA Take on E-cigarettes?
As health and quality concerns trouble the e-cigarette industry, experts and the public await the Food and Drug Administration (FDA)’s action to regulate the devices.
Parker Waichman Representing Another Louisiana Plaintiff in Actos Bladder Cancer Lawsuit
A Louisiana man has become the latest to claim that his taking the type 2 diabetes drug Actos resulted in developing bladder cancer. He has filed a lawsuit against the Japanese manufacturer of the drug and the marketer of it in the U.S., claiming they failed to warn about this ...
Older Hip Implant, Knee Replacement Patients Face Heart Attack Risk Following Surgery
An emerging report reveals that older hip implant and knee replacement patients face increased heart attack risks following surgery. The risk for acute myocardial infarction (AMI) was seen in the first two weeks after these surgical procedures.Power Morcellators can Worsen Uterine Cancers
A few years ago, the use of power morcellators in minimally invasive gynecologic surgeries did not arouse much concern. The tool, which cuts up large masses of tissue into smaller pieces, make it easier for surgeons to remove through small … Continue reading
Posted in Defective Medical Devices
Tagged cancerous fibroids, chemotherapy, FDA, fibroid surgery, Food and Drug Administration, Gynecology, hysterectomy, Medical Device Guardian’s Act, myomectomy, power morcellator cancer, power morcellator device, power morcellator lawsuit, Sugarbaker Procedure, Uterine Cancer, uterine fibroid removal, uterine sarcoma
