Tag Archives: Defective Medical Devices

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Long Island Car Crash Kills 1 Person, Injures 2 More

Long Island Car Crash Kills 1 Person, Injures 2 More

A car accident on LI left one person dead & two more critically injured. The crash occurred Monday in Deer Park on Straight Path, south of Sagamore Lane.

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Johnson & Johnson Marketing of Gynecare Prolift Transvaginal Mesh Raises More Questions

Johnson & Johnson and its Ethicon unit are again coming under scrutiny for the way it marketed its Gynecare ProLift transvaginal mesh product. According to a new report from Bloomberg News, Johnson & Johnson continued marketing the Gynecare ProLift device for months after it received a warning from the ...

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Study Finds Plavix May Only Benefit Smokers

An emerging study finds that blood thinner Plavix may only benefit smokers. Plavix (clopidogrel) is prescribed for the prevention of blood clots and heart attacks, and has been linked to serious side effects, including the heart attacks and strokes it is supposed to prevent, gastrointestinal and cerebral bleeding, bleeding ulcers, ...

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Medtronic Infuse Studies Faulted for Downplaying Side Effects

Medtronic Inc.’s published studies for its Infuse bone graft product may have downplayed serious side effects, according to an analysis published last year in The Spine Journal. The study, which drew on U.S. Food & Drug Administration (FDA) documents and other data sources, suggests that up to half of ...

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Actos Whistleblower Lawsuit Questions Avandia Researcher's Financial Ties to Takeda

A prominent researcher has been implicated in an alleged cover-up of Actos side effects, according to a report from TheHeart.org. An Actos whistleblower lawsuit unsealed earlier this year has alleged financial connections between the Cleveland Clinic’s Dr Steven Nissen and the maker of Actos “should be considered when analyzing Actos’s ...

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Stryker Metal Hip Implant Component Recall Bad News for Makers of Metal-on-Metal Hip Replacement Devices

Stryker’s recent recall of two metal hip implant components, the Rejuvenate Modular and ABG II modular-neck hip stems, may have dealt a serious blow to one of the key arguments medical device manufacturers have made to defend their metal-on-metal hip replacements. Facing thousands of lawsuits, the makers of ...

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Sleep Aids Can Increase Alzheimer’s Risk

A new study has found that over-the-counter sleeping aids and anti-allergy medicines can increase the risk of Alzheimer’s disease.

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FDA Questions Device Makers about Duodenoscope Cleaning Procedures

Following Deadly Outbreaks, FDA Questions Device Makers about Duodenoscope Cleaning Procedures

In light of a recent outbreak linked to contaminated duodenoscopes, the U.S. Food and Drug Administration (FDA) is questioning manufacturers about their methods for cleaning the devices, the New York Times reports. The specialized scopes, which have been linked to several outbreaks in recent years, most recently infected seven patients ...

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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 ...

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Estate of Kentucky Man Alleges Wrongful Death Due to Actos Bladder Cancer

National law firm, Parker Waichman LLP, just filed a lawsuit on behalf of the estate of a Kentucky man who developed bladder cancer and subsequently died, allegedly due to the use of diabetes drug, Actos. The lawsuit names Takeda Pharmaceuticals America, Inc., Takeda Pharmaceuticals USA, Inc., Takeda Pharmaceuticals North America, ...

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New Legislation Introduced in Light of Morcellator Risks

New Legislation Introduced in Light of Morcellator Risks

Safety concerns surrounding power morcellators have prompted lawmakers to team up with patient advocates and introduce new legislation. The Medical Device Guardians Act of 2016, which was introduced by U.S. Reps. Louise Slaughter, D-N.Y. and Michael Fitzpatrick, R-Pa., would require … Continue reading

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FDA, Medtronic issue advisory on SynchroMed drug infusion pump failures

The Food and Drug Administration has issued a warning that some Medtronic SynchroMed drug infusion pumps may malfunction and this could result in serious injuries or death. According to a Minnesota Public Radio report, the announcement from the agency is being … Continue reading

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Lawsuit filed against Medtronic for those injured by Entrust pacemaker, Sprint Fidelis leads

Three people who’ve been seriously injured as a result of defective cardiac defibrillators and their component parts manufactured by medical device maker Medtronic Inc. have sued the company for hiding data on the risks they posed to patients, and their … Continue reading

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Mirena® putting women at risk of suffering serious side effects

Women who opt for Mirena® as a contraceptive method are putting themselves at risk of very serious and sometimes life-threatening side effects. Mirena® is an intrauterine contraceptive that’s implanted in women and is designed to stay in the uterus for … Continue reading

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Metal hip surfacing recipients face high risk of early failures

A new study urges women and some men to avoid opting for an alternative to a hip replacement procedure, known as metal-on-metal hip resurfacing. According to a New York Times report on research gleaned from the National Joint Registry of … Continue reading

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DePuy ASR Hip Implants, Other Faulty Medical Devices Subject to Little FDA Oversight, Investigation Finds

A newly-published investigation from ProPublica has revealed that several questionable types of medical devices, including DePuy Orthopaedic’s recalled ASR hip implant, managed to make it to market without much scrutiny on the part of the U.S. Food & Drug Administration … Continue reading

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FDA Working on Barcode System to Track Medical Device Failures

The Food and Drug Administration (FDA) has proposed a barcode system that would allow the agency to track the failures of potentially defective medical devices with better efficiency. Using billing and medical records and tagged devices, the FDA believes it … Continue reading

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DePuy ASR Hip Implant Lawsuit Filed by Connecticut Woman

The first Connecticut lawsuit against the maker of the recalled, defective < "http://www.yourlawyer.com/topics/overview/DePuy-Hip-Implant-Recall-Johnson-and-Johnson">DePuy ASR hip implant has been filed. Patricia Sorrentino-Galello underwent a second hip replacement just three years after her original surgery at Milford Hospital, the CT Post reports. … Continue reading

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Recalled DePuy Hip Implant May Be Failing at Much Higher Rate than First Thought

How likely are premature failures of th< "http://www.yourlawyer.com/topics/overview/DePuy-Hip-Implant-Recall-Johnson-and-Johnson">e DePuy ASR XL Acetabular Hip Replacement System? When DePuy Orthopedics issued recalls for the ASR XL Acetabular Hip Replacement System and the ASR Hip Resurfacing System last August, the company said data … Continue reading

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Johnson & Johnson’s Animas Unit Recalls Insulin Pump Cartridges

Following a year of unprecedented recalls, another unit of embattled drug giant, Johnson & Johnson, is issuing a medical device recall, this time, for < "http://www.yourlawyer.com/practice_areas/defective_medical_devices">2.0 mL Animas Insulin Pump Cartridges. Some 2.0 mL insulin cartridges shipped between November 30, … Continue reading

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