Tag Archives: Stryker

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Newly-Filed Plavix Lawsuits Claim Drug Caused Gastrointestinal Bleeds, Cerebral Hemorrhage, and TTP

The manufacturer of Plavix continues to be named in lawsuits alleging the blood thinner caused some patients to suffer from serious bleeding side effects. Most recently, the national law firm of Parker Waichman LLP filed nine Plavix bleeding lawsuits in state court in New York.

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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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Whistleblower Wins Retaliation - Canaveral National Seashore

Whistleblower Wins Retaliation Lawsuit

A whistleblower who reported misconduct at Canaveral National Seashore has won a retaliation ruling against the U.S. Department of Interior, Florida Today reports.

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Federal DePuy ASR Hip Implant Trials Likely to Start This Year

It looks as though the first trials in the DePuy ASR hip implant multidistrict litigation could begin sometime later this year. According to a report from Bloomberg News, during a status conference held yesterday in Florida, attorneys for both plaintiffs and the defense told U.S. District Judge David Katz that ...

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First DePuy ASR Hip Implant Lawsuits Head to Trial in December, January

The first trials involving lawsuits filed against DePuy Orthopaedics by recipients of its recalled ASR Hip Implants will begin later this year, and early next year. The first is slated to start on December 3, 2012 in state court in Las Vegas, Nevada. A second DePuy ASR hip implant lawsuit ...

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Lawsuit Alleges Plavix Caused Oklahoma Man to Suffer Multiple Stomach Bleeds

Another lawsuit has been filed over adverse Plavix side effects. The lawsuit, filed by national law firm Parker Waichman LLP, alleges that the blood thinner, Plavix (clopidogrel), caused an Oklahoma man to suffer from multiple stomach bleeds.

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Federal Judge Certifies Medtronic Infuse Shareholder Class Action Lawsuit

A shareholder lawsuit alleging Medtronic Inc. illegally promoted the off-label use of its Infuse bone growth product has been granted class action status by U.S. District Judge Paul Magnuson of Minnesota. According to a report from Law360.com, the Medtronic Infuse off-label promotion lawsuit was filed by several institutional investors on ...

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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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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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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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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 , , , , |

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 , , , , |

Lawsuits Accuse Stryker of Hiding Problems with Spine Implant

spine

Fourteen lawsuits against device maker Stryker allege that Stryker’s CerviCore artificial discs are so dangerous that the company abandoned a clinical trial of the device and abandoned plans to obtain premarket approval (PMA) for the product. After the fourteenth suit … Continue reading

Posted in Defective Medical Devices, Health Concerns, Legal News | Tagged , , , , |

Stryker Recalls Fuhrman Pleural and Pneumopericardial Drainage Sets: Catheter May Break During Insertion

drainage

Stryker Sustainability Solutions has initiated a recall of the Fuhrman Pleural/Pneumopericardial Drainage Set, after two reports that the catheter included in the drainage set broke off in the pleural cavity. This is a Class 1 recall, the FDA’s most serious … Continue reading

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

Stryker Recalls Orthopedic Devices that May Have Been Damaged in Shipping

Stryker Recalls Orthopedic Devices

Medical device maker Stryker Corporation is recalling nearly 17,000 orthopedic implant devices because of potential of damage during shipping. The Food and Drug Administration (FDA) notice lists five devices included in the recall: the rHead lateral stem and Recon radial … Continue reading

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

Stryker Hip Settlement Program Payments to Begin This Summer

Stryker Hip Settlement Program Payments to Begin

Law firms representing patients in Stryker modular hip device litigation report that 95 percent of patients eligible for Stryker’s settlement program have enrolled and payments should begin later this summer. This settlement was established to provide compensation for patients injured … Continue reading

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

Stryker Hip Settlement Enrollment Deadline Extended

Stryker Hip Settlement Enrollment Deadline Extended

The deadline for hip implant recipients to enroll in the Stryker Orthopaedics Rejuvenate Hip System settlement has been extended to March 30, 2015. Patients who received a recalled ABG II Modular Hip System or Rejuvenate Modular Hip System still have … Continue reading

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

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