Category Archives: Product Recalls

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Fracking Should be Kept 600m From Aquifers, Study Says

New research on the safety of hydraulic fracturing (fracking) suggests new wells should not be dug within 600 meters of a water aquifer because underground fractures can extend about that far from a dug well. According to a report from UK’s The Guardian newspaper, researchers and geologists at Durham University have ...

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Stryker Metal Hip Implant Component Recall Bad News for Makers of Metal-on-Metal Hip Replacement Devices

Stryker’s recent recall of two metal hip implant components, the Rejuvenate Modular and ABG II modular-neck hip stems, may have dealt a serious blow to one of the key arguments medical device manufacturers have made to defend their metal-on-metal hip replacements. Facing thousands of lawsuits, the makers of ...

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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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Hip Replacement, Knee Implant Patients with Diabetes, Other Health Problems May Face Difficult Recoveries

Patients receiving hip replacement devices or knee implants may face a more complicated recovery if they are obese, or suffer from diabetes or other health woes. According to a new study published online in the journal Anesthesiology, at least 3% of all total hip or knee replacement patients will ...

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Johnson & Johnson’s Ethicon Division to End Sales of Gynecare Prolift, Three Other Transvaginal Mesh Devices

Johnson & Johnson’s Ethicon Inc. division revealed yesterday that it will end sales of its Gynecare Prolift device and three other transvaginal mesh products. The plan to stop selling the four products was set forth in a letter filed by the company in the Ethicon transvaginal mesh multidistrict litigation ...

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Crash on N.State Pkwy Kills Port Jefferson Station Man

Single-Car Crash on Northern State Parkway Kills Port Jefferson Station Man

81-year-old Port Jefferson Station man was killed in a crash at 4:57 a.m.. He lost control of the vehicle traveling west on Northern State Pkwy, on exit 42, Dix Hills.

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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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Actos, Avandia May Up Risk for Diabetic Macular Edema

A West Virginia man fitted with a metal-on-metal version of DePuy Orthopaedics’ Pinnacle Hip Implant System has filed suit against the company and its parent, Johnson & Johnson, alleging the device caused him to suffer pain and elevated cobalt levels. The Plaintiff is being represented by the national law ...

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J.J. Fuds, Inc. Pet Food Recalled - Listeria Contamination

J.J. Fuds, Inc. Pet Food Recalled Over Potential Listeria Contamination

J.J. Fuds, has recalled a specific lot of its J.J. Fuds Chicken Tender Chunks Pet Food over potential contamination with the dangerous, Listeria monocytogenes pathogen.

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MusclMasster Recalls Al-ER-G Capsules due to Ephedra

MusclMasster, LLC, is recalling all bottles of Al-Er-G Capsules due to the presence of Ephedra Herb, an ingredient that has been banned by the U.S. Food and Drug Administration (FDA). Dietary supplements that contain ephedrine alkaloids pose a risk of … Continue reading

Posted in Health Concerns, Product Recalls, Recalled Food Products |

Recalled Airbags May be Recycled to Replace Deployed Ones

According to Carfax, a service providing history on used vehicles that are being sold, as many as 750,000 airbags are replaced every year after an accident. Christopher Basso, a representative for Carfax said it is not uncommon to find recycled … Continue reading

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

Takata Pleads Guilty to Exploding Airbag Charges, More Cars Recalled

Takata Pleads Guilty to Exploding Car Airbag Charges

Takata Will Pay $1 Billion in Criminal Penalties Takata will pay $1 billion in criminal penalties related to its exploding airbag scandal, the Department of Justice announced. The company has agreed to plead guilty to charges of wire fraud, in … Continue reading

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Takata to Pay $1 Billion in Continuing Airbag Scandal

Automotive parts maker Takata Corporation will pay $1 billion in fines and settlements for concealing information about its defective airbags. The settlement includes $25 million to the U.S. government to settle one count of fraud, $850 million to automakers, and … Continue reading

Posted in Accident, Product Recalls, Recalled Vehicles |

General Motors’ Continuing Legal Trouble Over Defects and Recalls

General Motors, which recalled 2.6 million vehicles in 2014 over faulty ignition switches linked to injuries and death, faces continuing legal trouble over the defective ignition and switches and other defects. The company was accused of covering up ignition switch … Continue reading

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

St. Jude ICD Recall Is Deemed a Class I by Federal Regulators

St. Jude ICD Recall Is Deemed a Class I

St. Jude recently reported two patient deaths tied to early depletion of lithium batteries in St. Jude Medical Implantable Cardioverter Defibrillators (ICD) and Cardiac Resynchronization Therapy Defibrillators (CRT-D). The U.S. Food and Drug Administration (FDA) and St. Jude issued an … Continue reading

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

Teleflex Medical Recalls Tracheostomy Tube Set Due to Possible Disconnection During Use

Teleflex Medical Recalls Tracheostomy Tube Set

Teleflex Medical has issued a recall for the Willy Rusch Tracheostomy Tube Set because the connector may disconnect from the tracheostomy tube during use on a ventilated patient. If the connector detaches from the tracheostomy tube shaft during use, the … Continue reading

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HeartWare International Heart Pump Subject to FDA Class 1 Recall

HeartWare International Heart Pump Subject to FDA Recall

Medtronic has announced that the U.S. Food and Drug Administration (FDA) has classified two global voluntary recalls of HeartWare International’s HeartWare Ventricular Assist Device (HVAD) as Class 1 recalls. A class 1 recall is the FDA’s most serious recall category, … Continue reading

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Lunchables Recalled Due to Undeclared Allergens, Misbranding

Lunchables Recalled Due to Undeclared Allergens, Misbranding

Kraft Heinz is recalling its ready-to-eat “Lunchables Ham and American Cracker Stackers because it is misbranded and contains undeclared allergens, including wheat and soy. These ingredients, which can cause a life-threatening allergic reaction in some individuals, were not listed on … Continue reading

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Nestlé Drumstick Ice Cream Cones Recalled

Nestlé Drumstick Ice Cream Cones Recalled

A voluntary recall has been issued for Nestlé Drumstick Club 16 count Variety Pack and 24 count Vanilla Pack (with cones marked for easy individual sale). Nestlé USA recalled the product because contact surfaces of equipment tested positive for Listeria … Continue reading

Posted in Food Poisoning, Listeria, Product Recalls, Recalled Food Products | Tagged , , , |

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