Tag Archives: Medical Device Guardian’s Act
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Oklahoma Woman Latest to Head to Court Over Alleged DePuy ASR Hip Implant Injuries
Lawsuits filed by alleged victims of DePuy Orthopaedics’ recalled ASR hip replacement devices continue to pile up in the multidistrict litigation currently underway in U.S. District Court, Northern District of Ohio. Most recently, a woman from Pryor, Oklahoma, filed suit alleging complications caused by a DePuy ASR hip implant ...
Research Study Confirms Fracking as Cause of Ohio Earthquakes
Fracking operation near Poland Township, Ohio, activated a previously unknown fault in the, causing 77 earthquakes with magnitudes ranging from 1.0 to 3.0 in March 2014.
Exposure to Common Pesticide May Increase ADHD Risk
A new study has found that exposure to a common household pesticide may increase the risk of attention deficit hyperactivity disorder (ADHD) in children.
FDA Gives 7 Companies Go Ahead To Market Generic Plavix
The U.S. Food & Drug Administration (FDA) just gave seven companies the go-ahead to market generic Plavix. Plavix is a blood thinner prescribed for the prevention of blood clots, heart attacks, and which has been linked to serious side effects such as the heart attacks and strokes it is supposed to ...
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.
U.K. Regulators Issue Additional Guidance for Metal-on-Metal Hip Implant Recipients
Regulators in the U.K. are once again issuing advice to doctors and other healthcare professionals involved in the follow-up of patients with metal-on-metal hip replacement devices. In an alert issued by the Medicines and Healthcare products Regulatory Agency (MHRA), guidance is provided for four groups of metal-on-metal hip implant ...
Metal-on-Metal Hip Replacement Concerns Grow in Canada
Canadian patients and doctors are voicing more concerns about metal-on-metal hip replacements, as health regulators around the world continue to investigate the safety of the devices. According to a report from the CBC, four companies have recently either recalled or suspended sales of metal-on-metal hip replacement devices, while a number ...
FDA Panel Takes up Metal-on-Metal Hip Implant Safety Today
The Food and Drug Administration (FDA) is convening a meeting starting today to help decide the future of metal-on-metal hip implants following high-profile recalls and mounting questions about their overall safety.
Trial over Ethicon Transvaginal Mesh Begins in California
Pelvic mesh devices have become the subject of safety concerns in recent years amidst reports that they can cause serious, sometimes permanent injuries.
New York City Council Calls for Zadroga Act to be Renewed
New York City Council members are calling for the Zadroga Act, which provides compensation and medical treatment to 9/11 victims, to be renewed. According to press release issued Jan. 7, a resolution was introduced by Council Member Margaret Chin, Council Speaker Melissa Mark-Viverito and Council Members Paul Vallone and I. ...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
