Monthly Archives: December 2009

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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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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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National Law Firms Calls for More FDA Action on Actos Bladder Cancer Threat

A national law firm is not satisfied with the way the U.S. Food & Drug Administration (FDA) has handled warnings regarding Actos (pioglitazone) bladder cancer risks. In a statement published today, Parker Waichman LLP called on the FDA to compel Takeda Pharmaceuticals, the maker of the type 2 diabetes drug, ...

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Birth Control Shot Depo-Provera may Increase HIV Risk

Birth Control Shot Depo-Provera may Increase HIV Risk, Study Suggests

A new study has linked the use of Depo-Provera (medroxyprogesterone acetate), an injectable type of birth control, to an increased risk of HIV infection.

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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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Another Metal-on-Metal Hip Replacement Lawsuit Filed in DePuy ASR Hip Implant Litigation

A vital food safety program was saved from budget cuts this week, enabling the country’s largest—although considered by experts to be far too small—produce-safety testing program to continue.

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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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Lawsuits over DePuy ASR Metal-on-Metal Hip Implants Continue to Mount

DePuy Orthopaedics and its parent, Johnson & Johnson, continue to be hit with lawsuits over recalled metal-on-metal DePuy ASR hip implants. Just yesterday, the national law firm of Parker Waichman LLP announced it had filed yet another DePuy ASR hip implant lawsuit, this time on behalf of a Virginia resident ...

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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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Dehumidifiers Recalled For Burn Hazard

About < "http://www.yourlawyer.com/practice_areas/product_liability">98,000 Portable Dehumidifiers, which were manufactured by LG Electronics Tianjin Appliance Co., of China, have been recalled due to fire and burn hazards, the U.S. Consumer Product Safety Commission (CPSC) and Health Canada just announced. The power connector … Continue reading

Posted in Legal News |

Firm Settles With DOJ Over Unapproved Medical Device

Spectranetics Corporation, a < "http://www.yourlawyer.com/practice_areas/defective_medical_devices">medical device manufacturer, located in Colorado Springs, Colorado, has agreed to pay the United States $4.9 million in civil damages and a $100,000 forfeiture to resolve claims against the company, the Justice Department just announced, said … Continue reading

Posted in Defective Medical Devices, Product Recalls, Recalled Medical Devices |

Sprint Fidelis Problems Weigh On Medtronic

We have long been writing about the dangerous, sometimes deadly, issue regarding < "http://www.yourlawyer.com/practice_areas/defective_medical_devices">defective cardiac device leads. Now, a report out by UBS Investment Research announced that, “lead failures could accelerate over time,” said Med City News. Lead wires are … Continue reading

Posted in Defective Medical Devices, Medtronic Defibrillators |

E. coli Tainted Beef Served In Restaurants Sickens 21

Earlier this week we wrote that an < "http://www.yourlawyer.com/practice_areas/food_poisoning">E. coli outbreak prompted the recall of 248,000 pounds of beef products produced by National Steak and Poultry, of Owasso, Oklahoma. The U.S. Department of Agriculture’s (USDA) Food Safety & Inspection Service … Continue reading

Posted in E. Coli, Food Poisoning |

Lead Paint Violation Prompts Recall Of Wooden Toys

About 300 < "http://www.yourlawyer.com/practice_areas/product_liability">Wooden Skill Ball Toys distributed by Kendamaspot LLC, of Redmond, Washington have been recalled, the U.S. Consumer Product Safety Commission (CPSC) just announced. The surface paint coating on the ball contains excessive levels of lead, violating the … Continue reading

Posted in Children's Toys, Defective Products, Health Concerns, Toxic Substances |

Safety 1st Disney, Eddie Bauer Play Yards Recalled

A large recall of about 213,000 < "http://www.yourlawyer.com/practice_areas/product_liability">Safety 1st Disney Care Centerâ„¢ Play Yards and Eddie Bauer Complete Care Play Yards has been announced, said the U.S. Consumer Product Safety Commission (CPSC). The recalled Safety 1st Disney Care Centerâ„¢ Play … Continue reading

Posted in Legal News |

FDA to Study Effect Of Prescription Drugs on Pregnant Women

A new research program called the Medication Exposure in Pregnancy Risk Evaluation Program (MEPREP) will fund research to study the effects of < "http://www.yourlawyer.com/practice_areas/defective_drugs">prescription medications used during pregnancy, the U.S. Food and Drug Administration (FDA) just announced. The program is … Continue reading

Posted in Health Concerns, Pharmaceuticals |

Salmonella Hazelnut Recalls Continue

Janzen Farms, Dayton, Oregon is recalling hazelnut kernels because the product has the potential to be contaminated with < "http://www.yourlawyer.com/practice_areas/food_poisoning">Salmonella, the U.S. Food and Drug Administration (FDA), just announced. The recalled hazelnut kernels were sold in November and December 2009 … Continue reading

Posted in Food Poisoning, Salmonella |

FDA Slammed Over Heart Device Trials

The U.S. Food and Drug Administration (FDA) has been criticized by two prominent medical journals over how it approves < "http://www.yourlawyer.com/practice_areas/defective_medical_devices">cardiovascular medical devices, says the Wall Street Journal. The journals accused the FDA of releasing some devices to market based … Continue reading

Posted in Defective Medical Devices |

FDA Misses BPA Deadline Again

For the third time this year, the U.S. Food and Drug Administration (FDA) will miss its own deadline on advising the public on the safety of products manufactured with the controversial chemical < "http://www.yourlawyer.com/practice_areas/toxic_substances">bisphenol A—BPA—reports the Milwaukee-Wisconsin Journal Sentinel (JSOnline). … Continue reading

Posted in Health Concerns, Toxic Substances |

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