Category Archives: Product Recalls

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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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Canadian Study Confirms Actos Bladder Cancer Risk

A new study conducted by Canadian researchers has found that users of the type 2 diabetes drug, Actos (pioglitazone), may face a higher risk of developing bladder cancer than first thought. The study, published in the British Medical Journal, found that taking Actos for two years doubles the likelihood ...

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FDA Advisors Set to Examine Metal-on-Metal Hip Implant Safety Concerns

Thousands of people with metal-on-metal hip implant devices could soon get some answers from the U.S. Food & Drug Administration (FDA) about the dangers they face. Tomorrow, the agency will convene a panel of outside medical experts to examine the safety record of metal-on-metal hip replacements, and recommend the ...

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FDA Advisory Panel Wrestling with Metal-on-Metal Hip Replacement Safety

An advisory panel for the U.S. Food & Drug Administration (FDA) began a highly-anticipated meeting yesterday to discuss the safety of metal-on-metal hip implants. Among other things, the panel of outside experts is being asked to make recommendations regarding the best practices for monitoring patients with metal-on-metal hip replacements. ...

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FDA Metal-On-Metal Hip Replacement Investigation Is Flawed, Researchers Say

The U.S. Food & Drug Administration’s (FDA) metal-on-metal hip replacement investigation is flawed, according to researchers.

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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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New York City Council Calls for Zadroga Act to be Renewed

New York City Council Calls for Zadroga Act to be Renewed

New York City Council members are calling for the Zadroga Act, which provides compensation and medical treatment to 9/11 victims, to be renewed.

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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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Image Source: wisegeek.com

Trial over Ethicon Transvaginal Mesh Begins in California

Pelvic mesh devices have become the subject of safety concerns in recent years amidst reports that they can cause serious, sometimes permanent injuries.

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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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