Category Archives: Product Recalls

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Warning for Medtronic InterStim Neurostimulation Devices

Australian Health Agency Issues Warning for Battery Problem with Medtronic InterStim Neurostimulation Devices

Warning for Medtronic InterStim Neurostimulation DevicesTGA has issued a safety warning for InterStim and InterStim II neurostimulation devices, because of possible early depletion of the battery.

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Actos Bladder Cancer Lawsuits Continue, New Complaint Filed by Tennessee Resident

Actos bladder cancer lawsuits continue, with a new complaint filed by a resident of Tennessee. The national law firm, Parker Waichman LLP, represents the Tennessee man who alleges that Actos caused his bladder cancer.

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Fracking Boom Changing Way of Life in Pennsylvania's Northern Tier

In just a few years, the impact of hydraulic fracturing (fracking) drilling on northeastern Pennsylvania is hard to miss. Thousands of natural gas wells have been opened in that area specifically in the last five years as companies look to exploit the vast Marcellus shale formation about two miles below the ...

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Research Study Confirms Fracking Cause of Ohio Earthquakes

Research Study Confirms Fracking as Cause of Ohio Earthquakes

Fracking operation near Poland Township, Ohio, activated a previously unknown fault in the, causing 77 earthquakes with magnitudes ranging from 1.0 to 3.0 in March 2014.

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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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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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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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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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Metal-on-Metal Hip Replacement Concerns Grow in Canada

Canadian patients and doctors are voicing more concerns about metal-on-metal hip replacements, as health regulators around the world continue to investigate the safety of the devices. According to a report from the CBC, four companies have recently either recalled or suspended sales of metal-on-metal hip replacement devices, while a number ...

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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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Slap Bracelets Recalled due to Laceration Hazard

On September 7, the Consumer Product Safety Commission (CPSC) published a recall regarding bracelets sold with storybooks due to a potential laceration hazard. Studio Fun International recalled approximately 86,000 slap bracelets that were sold in the United States and in … Continue reading

Posted in Children's Toys, Health Concerns, Product Recalls |

Faulty St. Jude Riata Defibrillators may have Fatal Consequences

Patients who still have recalled St. Jude Defibrillators leads in their chests have many reasons to be vigilant. Premature insulation failure in the recalled device has been tentatively linked to polymicrobial endocarditis, a serious, often deadly condition that leads to … Continue reading

Posted in Defective Medical Devices, Health Concerns, Product Recalls, Recalled Medical Devices, St. Jude Defibrillators |

2018 Chevrolet Equinox, GMC Terrain, GMC Acadia Recalled

Approximately 2,900 vehicles of the model-year 2018 Chevrolet Equinox, 2018 GMC Terrain SUVs, and 2017-1018 GMC Acadia SUVs have been recalled, according to the Daily Hornet. The problem is that the right front intermediate driveshaft may fracture. If the driveshaft … Continue reading

Posted in Defective Products, Health Concerns, Legal News, Product Recalls, Recalled Vehicles |

Bestherbal Herbal Coffee Recalled Over Possible Tainting with Viagra-Like Substance

Bestherbal Coffee Recalled New of Kopi Jantan Tradisional Natjral Herbs Coffee Bestherbs Coffee LLC just has issued a recall for its “New of Kopi Jantan Tradisional Natural Herbs Coffee” following an analysis by the U.S. Food and Drug Administration (FDA) … Continue reading

Posted in Defective Products, Product Recalls, Recalled Food Products |

Thousands of Propane Cylinders Recalled Because of Fire Risk

On July 13, 2017, the U.S. Consumer Product Safety Commission (CPSC) in conjunction with Health Canada announced the recall of certain refillable propane cylinders that pose a risk of explosion and fire. YSN Imports, of Gardena, California, which distributes the … Continue reading

Posted in Product Recalls |

Samsung Galaxy Note 4 Recall due to Potentially Hazardous Batteries

The most recent unfortunate news for Samsung’s beleaguered line of Galaxy Note smartphones is that over 10,000 refurbished batteries for the Note 4, a three-year-old phone, are being recalled due to a risk of overheating, with the potential of fires … Continue reading

Posted in Cellular Phone, Defective Products, Product Recalls |

Cook Medical Recalls Medical Device due to Blood Clot Risk

The U.S. Food and Drug Administration (FDA) has identified the Cook Medical Zenith Alpha Thoracic Endovascular Graft as a Class I recall, the most serious type of recall where there is a “reasonable probability that the use of or exposure … Continue reading

Posted in Defective Medical Devices, Defective Products, Health Concerns, Legal News, Product Recalls, Recalled Medical Devices |

Papaya Salmonella Victims Increase to 141 with More Possible

As of August 11, 2017, the Centers for Disease Control (CDC) is reporting that 141 people in nineteen states have confirmed cases of strains of salmonella traced back to papayas imported from Mexico. Victims range in age from 1 to … Continue reading

Posted in E. Coli, Food Poisoning, Food Products, Health Concerns, Listeria, Recalled Food Products, Salmonella |

Endo Agrees to Additional $775M Settlement for a Total of $2.6B

As of August 7, 2017, Endo International has agreed to set aside an additional $775 million to resolve the company’s remaining mesh lawsuits’ allegations related to the Transvaginal Mesh (TVM) Multidistrict (MDL) Litigation pending in the U.S. district Court of … Continue reading

Posted in Defective Medical Devices, Defective Products, Health Concerns, Product Recalls, Recalled Vehicles, Transvaginal mesh |

General Motors Recalls 800,000 Trucks due to Power Steering Defects

Nearly 800,000 pickup trucks are being recalled by General Motors because they may suddenly lose power steering while the truck is being driven, and the sudden steering jolt may cause drivers to lose control of the vehicle, reports Fortune. About … Continue reading

Posted in Defective Products, Motor Vehicles, Product Recalls, Recalled Vehicles |

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