Tag Archives: hernia

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Bleeding Side Effects of Pradaxa, Xarelto Have Some Doctors Concerned

Some heart doctors are raising concerns about a new class of heart drugs that include Pradaxa. Recently, a number of doctors interviewed by Reuters said they were hesitant to prescribe Pradaxa, as well as another blood thinner called Xarelto, because of concerns regarding the risk of stroke, serious bleeding ...

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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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Cancer Groups Call for E-cigarettes Regulation/Research

Two-Leading-Cancer-Groups-Issue-Call-for-Regulation-of-E-cigarettes-and-Research-on-Health-Risks

The American Society of Clinical Oncology & the American Association for Cancer Research called for government regulation & research of e-cigarettes on health effects.

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Smokers More Vulnerable to Joint Replacement Failures

People who smoke cigarettes before and after receiving a total joint replacement, such as a hip replacement device or knee implant, are far more likely to endure revision surgeries on those implants than people who don’t smoke.

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West Virginia Man Claims Metal-on-Metal DePuy Pinnacle Hip Replacement Led to Pain, Elevated Cobalt Levels

A West Virginia man fitted with a metal-on-metal version of DePuy Orthopaedics’ Pinnacle Hip Implant System has filed suit against the company and its parent, Johnson & Johnson, alleging the device caused him to suffer pain and elevated cobalt levels. The Plaintiff is being represented by the national law ...

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Hip Replacement, Knee Implant Patients with Diabetes, Other Health Problems May Face Difficult Recoveries

Patients receiving hip replacement devices or knee implants may face a more complicated recovery if they are obese, or suffer from diabetes or other health woes. According to a new study published online in the journal Anesthesiology, at least 3% of all total hip or knee replacement patients will ...

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FDA Urged to Ban Powdered Caffeine

FDA Urged to Ban Powdered Caffeine

Pennsylvania Senator Robert Casey has written to the Food and Drug Administration (FDA) to urge the agency to ban powdered caffeine, a dietary supplement.

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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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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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Atrium C-Qur Hernia Mesh Complications and Lawsuits

Atrium C-Qur Hernia Mesh Complications and Lawsuits

A woman recently filed a lawsuit against Atrium Medical, the manufacturers of the Atrium C-Qur hernia mesh, alleging severe pain and injury after the mesh was used during an open repair of her ventral (abdominal) hernia in 2011. According to … Continue reading

Posted in Defective Medical Devices, Transvaginal mesh | Tagged , , , , |

Ethicon Sued over Physiomesh Hernia Mesh, Withdrawn from Market

Physiomesh Withdrawn Due to High Rates of Revision

Physiomesh Withdrawn Due to High Rate of Recurrence, Revision Ethicon, a unit of Johnson & Johnson, is being sued over its Physiomesh Composite Mesh used for hernia repairs. The company withdrew the product from the market in May 2016 due … Continue reading

Posted in Defective Medical Devices | Tagged , , , , |

Johnson & Johnson’s Ethicon Recalls Physiomesh Hernia Mesh

J&J’s Ethicon Recalls Physiomesh Hernia Mesh

Physiomesh Recalled Due to High Failure Rates Ethicon, a Johnson & Johnson unit, is recalling its Physiomesh because studies show that patients are undergoing higher rates of revision surgery compared to other mesh devices. Physiomesh flexible composite hernia mesh is … Continue reading

Posted in Defective Medical Devices | Tagged , , , , , |

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