Category Archives: Medtonic Infuse

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1,000+ Australians Join DePuy ASR Hip Implant Class Action Lawsuit

A class action lawsuit filed in Australia over DePuy Orthopaedics’ recalled metal-on-metal ASR Hip Implants has signed up more than 1,000 plaintiffs. The attorneys representing the Australian ASR Hip Implant lawsuit plaintiffs recently told The Courier-Mail that damages in the lawsuit are expected to be worth more than $200 million. One ...

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Government Penalizes 721 Hospitals for High Rates of Infections, Injuries

Medicare is reducing payments to 721 hospitals, one out of every seven hospitals in the nation, for having high rates of “hospital-acquired” conditions (HAC.

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Actos, Avandia May Up Risk for Diabetic Macular Edema

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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First Bard Avaulta Transvaginal Mesh Lawsuit Scheduled for February Trial in MDL

The first test trials in the federal C.R. Bard Avaulta transvaginal mesh litigation will most likely start next year, according to a report from Bloomberg News. About 600 lawsuits involving Bard Avaulta transvaginal mesh products are currently pending in the multidistrict litigation underway Charleston, West Virginia. U.S. District Judge Joseph ...

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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.

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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 (FDA).

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Medtronic Infuse Lawsuit Alleges Off-Label Use Cause Painful Complications

A man in Louisiana has filed suit against Medtronic Inc. over injuries allegedly cause by off-label use of its Infuse Bone Graft product. The plaintiff, who received Infuse during transforaminal spinal lumbar fusion surgery, claims that the bone growth protein caused unwanted bone growth along his spine, worsening the back ...

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Study Linking Z-Pak to Increased Death Risk Being Reviewed by FDA

The U.S. Food & Drug Administration (FDA) is reviewing a new study that reported an increased risk of sudden, heart-related deaths among people using the antibiotic Zithromax (azithromycin), known popularly as Z-Pak. In a statement issued late yesterday, the FDA said patients being treated with Zithromax should not stop taking ...

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FDA Warning for Bone Graft Products in Patients Under 18

FDA Safety Warning for Bone Graft Products in Patients Under 18

FDA issued safety alerts to patients, parents & guardians, bone graft devices w/recombinant proteins or synthetic peptides not to be the first treatment for 18 & under.

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Stanford University Study: Medtronic Infuse Bone Graft Device Increases Cancer Risks

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A new Stanford University study has found that use of Medtronic’s Infuse increases new cancer risks. According to a Stanford University study published in the September 4, 2013, edition of The Journal of Bone & Joint Surgery, a large dose—at … Continue reading

Posted in Defective Medical Devices, Medtonic Infuse |

Medtronic Bid to Dismiss InFuse Case Denied

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Medtronic Inc.’s bid for preemption was just denied by a federal judge. The case involved the device maker’s highly controversial InFuse bone graft product. The Arizona judge rejected Medtronic’s arguments that federal law preempted a lawsuit brought over claims that … Continue reading

Posted in Defective Medical Devices, Medtonic Infuse |

Judge Blocks Medtronic InFuse Suits, Plaintiffs to Re-File Cases Alleging Fraud

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Although a lower court Illinois state court judge very recently denied device maker, Medtronic Inc.’s, bid to dismiss a lawsuit brought over its InFuse bone graft product, a Minneapolis judge did grant Medtronic’s motion to dismiss the InFuse claims there. … Continue reading

Posted in Defective Medical Devices, Medtonic Infuse |

Industry Promises Increased Transparency, Medtronic InFuse Debacle Cited

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Some of the world’s largest drug makers have promised to release detailed information about their pharmaceutical products, such as Medtronic’s InFuse, to external researchers. While many are happy with the move, others point out that this might be a way … Continue reading

Posted in Defective Medical Devices, Medtonic Infuse, Medtronic Infuse |

Medtronic’s Motion to Dismiss InFuse Lawsuit Denied

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An Illinois state court judge just denied device maker, Medtronic Inc.’s, bid to dismiss a lawsuit brought over its InFuse bone graft product. The lawsuit included allegations that InFuse caused a patient to undergo additional surgery that led to permanent … Continue reading

Posted in Defective Medical Devices, Medtonic Infuse, Medtronic Infuse |

Pending Sunshine Act to Focus on Allegedly Fraudulent Financial Ties Between Physicians and Industry

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On August 1, the Physician Payment Sunshine Act provision of the Affordable Care Act will go into effect. The Act is meant to highlight allegedly bogus relationships between physicians and pharmaceutical firms and medical device manufacturers. As we’ve long stressed, … Continue reading

Posted in Defective Medical Devices, Medtonic Infuse, Medtronic Infuse |

Increased Transparency in Medicine Coming

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When approved by the U.S Food and Drug Administration in 2002, Medtronic’s bone graft product, InFuse, was seen as a medical breakthrough. InFuse eliminated the need to remove patient bone from the hip in spinal fusions and could, instead, use … Continue reading

Posted in Defective Medical Devices, Medtonic Infuse, Medtronic Infuse |

Injured InFuse Users Working Toward Their Day in Court

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Hundreds of people allegedly injured following procedures involving Medtronic’s InFuse are utilizing a different legal approach. The arguments planned include that the U.S. Food and Drug Administration (FDA) issued a warning in 2008 to physicians concerning “life-threatening complications” from unapproved … Continue reading

Posted in Defective Medical Devices, Medtonic Infuse, Medtronic Infuse |

Do Consumers Know the Risks of Medtronic InFuse? Are Consumers Aware of Safer Options?

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Medtronic’s bone graft product, InFuse, is a synthetic, or genetically engineered, recombinant human Bone Morphogenetic Protein (rhBMP-2) that was approved by the U.S. Food & Drug Administration (FDA) in 2002 for specific uses. Meant to stimulate spine growth in patients … Continue reading

Posted in Defective Medical Devices, Medtonic Infuse, Medtronic Infuse |

Medtronic Shareholders File Lawsuit Amid InFuse® Scandal

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  Device maker, Medtronic, is the focus of another shareholder lawsuit over its InFuse® bone growth product. Shareholders filed the lawsuit against Medtronic and some of its shareholders accusing them of intentionally minimizing potential dangers associated with InFuse® so that … Continue reading

Posted in Defective Medical Devices, Medtonic Infuse, Medtronic Infuse |

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