Category Archives: Metal Hip Implants

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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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What Action Will the FDA Take on E-cigarettes?

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.

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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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Tennessee Resident Files Pradaxa Bleeding Lawsuit Following Cerebral Hemorrhage

A man from Tennessee has filed a lawsuit against the maker of Pradaxa, claiming that the blood thinner caused him to suffer a cerebral hemorrhage. The complaint alleges Boehringer Ingelheim Pharmaceuticals, Inc. concealed knowledge that Pradaxa can cause Serious, life-threatening bleeds, and did not warn that Pradaxa bleeding side effects ...

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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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Transvaginal Mesh Lawsuit Trial

$5.5 Million Awarded to Plaintiffs in First Transvaginal Mesh Lawsuit Trial

An award of $5.5 million has been made in the first trial over a transvaginal mesh lawsuit. The jury found against medical device maker, C.R. Bard, and its Avaulta Plus transvaginal mesh. The jury agreed that Bard’s Avaulta Plus transvaginal mesh caused numerous and painful injuries in a California woman. ...

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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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Study Suggests Hormonal Contraceptives Linked to Brain Tumor

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.

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Boston Scientific Transvaginal Mesh

Tennessee Woman Alleges Boston Scientific Transvaginal Mesh Product Caused Painful Injuries

More reports of painful injuries are being linked to transvaginal mesh. This time, a Tennessee woman has filed a lawsuit against Boston Scientific over its Advantage Transvaginal Mid-Urethral Sling System.

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Retailers Accused of Selling Fraudulent Herbal Supplements

Major Retailers Accused of Selling Fraudulent Herbal Supplements

The NYS attorney general’s office has accused four national retailers of selling fraudulent dietary supplements.

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Mixed Metals are Focus of Stryker LFIT V40 Hip Implant Litigation

The Stryker Corporation is facing parallel litigations in Boston and New Jersey defending its LFIT Anatomic CoCr V40 Femoral Head (Cobalt Chromium V40) with allegations that the metal-on-metal ball and joint hip implant has a design defect causing it to … Continue reading

Posted in Defective Medical Devices, Depuy, Health Concerns, Metal Hip Implants, Recalled Medical Devices |

Stryker Hip Implant Failure Lawsuits Update

State-Based Stryker Lawsuits Consolidated in New Jersey The New Jersey Supreme Court recently approved consolidation of all pending and future state-based hip replacement implant failure lawsuits brought against Stryker Corp. subsidiary, Howmedica Osteonics Corp.. within a multicounty legislation. The medical device products … Continue reading

Posted in Defective Medical Devices, Metal Hip Implants |

Defective Stryker Hip Implant Lawsuits Consolidate

Defective Stryker Hip Implant Lawsuits Consolidate

In the interest of expedience, dozens of Stryker hip implant lawsuits will be consolidated as agreed upon by the U.S. Judicial Panel on Multidistrict Litigation (JPML). The transfer of nearly three dozen pending cases involve alleged defects in a prosthetic … Continue reading

Posted in Defective Medical Devices, Metal Hip Implants | Tagged , , , , |

Another DePuy Pinnacle MoM Lawsuit Filed

Pinnacle Metallosis Lawsuits Added To Texas MDL A new lawsuit has been filed against DePuy Orthopedics and Johnson & Johnson over an allegedly failed Pinnacle Acetabular Cup system. DePuy Orthopaedics is a unit of Johnson & Johnson. The Pinnacle metal-on-metal … Continue reading

Posted in Defective Medical Devices, Depuy, Metal Hip Implants |

Stryker Hip Accolade and Rejuvenate Settlement Extended

Some Additional Plaintiffs Are Now Included in the Revised Stryker Settlement Agreement Patients implanted with specific Stryker hip replacements who were ineligible for the initial 2014 Stryker hip settlement may now be eligible for the expanded settlement agreement. Specifically, patients … Continue reading

Posted in Defective Medical Devices, Metal Hip Implants |

Johnson & Johnson Hit with $1 Billion Verdict in DePuy Pinnacle Hip Case

On November 30, a federal jury in Dallas, Texas ordered Johnson & Johnson and its DePuy Orthopaedics unit to pay more than $1 billion to six plaintiffs who said they were injured by Pinnacle hip implants. The jury found that … Continue reading

Posted in Defective Medical Devices, Depuy, Metal Hip Implants |

Stryker Faces Mounting Defective Hip Implant Lawsuits

Medical device maker Stryker and other leading manufacturers of metal-on-metal hip implants have received thousands of complaints from both doctors and patients that their devices, including the Stryker LFIT, are defective and prone to high rates of failure. According to … Continue reading

Posted in Defective Medical Devices, Metal Hip Implants |

Stryker LFIT Metal-on-Metal Hip Component Safety Concerns

Stryker LFIT Metal-on-Metal Hip Component Safety Concerns

Stryker LFIT CoCr V40 Femoral Heads Recalled in Canada, “Hazard Alert” Issued in Australia Regulators in Canada and Australia recently took action regarding a metal-on-metal hip implant component, the LFIT CoCr V40 Femoral Heads. Metal-on-metal hip implants have been the … Continue reading

Posted in Defective Medical Devices, Metal Hip Implants | Tagged , , , , |

Plaintiffs in DePuy Pinnacle Litigation Say J&J Lied about Hip Implant Safety

Plaintiffs in DePuy Pinnacle MDL Say J&J Lied about Implants

On the first day of the third bellwether trial over the DePuy Pinnacle metal-on-metal implants, jurors heard arguments that DePuy and parent company Johnson & Johnson deceived physicians and patients about the safety of the hip device. The company allegedly … Continue reading

Posted in Defective Medical Devices, Depuy, Metal Hip Implants | Tagged , , , , |

Stryker Recalls Metal Hip Implant Component in Canada

Stryker Recalls Metal Hip Implant Component in Canada

Stryker Orthopaedics may be facing a new wave of litigation over a recently recalled metal hip implant component. The Stryker LFIT CoCr V40 femoral heads were recalled in Canada. According to an Aug. 24, 2016 recall alert posted on Health … Continue reading

Posted in Defective Medical Devices, Metal Hip Implants | Tagged , , , , |

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