Category Archives: Product Recalls

Featured Stories

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. ...

Read More

Scientist Calls for Federal Regulations for Fracking Pollution

Hydraulic fracturing (fracking) drilling should be governed by federal regulations because its pollution has no awareness of state boundaries.

Read More

Medtronic Plans Layoffs, as Infuse Bone Graft Controversy Continues to Weigh on Spinal Business

Medtronic’s spinal division continues to take a huge hit thanks to the controversy surrounding its Infuse Bone Graft product. According to a report from MassDevice.com, the company’s latest earnings report stated that the division saw Infuse sales decline 26% in the first quarter of 2012, and now Medtronic is talking ...

Read More

British Health Agency Strengthens Warnings about Valproate

British Health Agency Strengthens Warnings about Valproate Risk in Pregnancy

Statement issued urging healthcare professionals to give women information on birth defects when Depakote and other valproate medicines are used during pregnancy.

Read More

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 ...

Read More

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.

Read More

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.

Read More

Lawsuit Alleges Bi-Lateral DePuy ASR Hip Implant Resulted in Elevated Chromium and Cobalt Levels, Need for Revision Surgery

DePuy Orthopaedics and its parent, Johnson & Johnson, continue to be named in lawsuits by metal-on-metal hip replacement recipients who suffered severe injuries, including elevated chromium and cobalt levels, allegedly due to recalled ASR hip implant devices. Most recently, the national law firm of Parker Waichman LLP filed suit on ...

Read More

Older Patients Face Heart Attack Risk Following Surgery

Older Hip Implant, Knee Replacement Patients Face Heart Attack Risk Following Surgery

An emerging report reveals that older hip implant and knee replacement patients face increased heart attack risks following surgery. The risk for acute myocardial infarction (AMI) was seen in the first two weeks after these surgical procedures.

Read More

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 |

© 2005-2018 Parker Waichman LLP ®. All Rights Reserved.