Toyota has agreed to pay $16 million in penalties after the government contended that Toyota knowingly refrained from disclosing the sticky gas pedal defect to the public and did not take action to protect the public from harm. Toyota’s agreement does not mean that the company admits to wrongdoing. However,…
Guidant, LLC, maker of a cardiac defibrillator, pled guilty to criminal violations of the Food and Dug Administration Cosmetic Act which requires that medical device companies disclose risks of serious injury and death that are associated with their products. The Guidant defibrillator was used in cardiac surgery to produce a…
Stuffed animals, rain ponchos and play jewelry are some of the Toy products that Daiso California LLC had been selling before a recall. The risks associated with their products included strangulation from the rain ponchos, lead poisoning from the jewelry, and choking from the stuff animals. Since Daiso California LLC…
Reglan, manufactured by Baxter Healthcare Corporation, has long been used in over 2 million children and adults for the treatment of gastrointestinal conditions such as diabetic gastroparesis disease and gastroesophageal reflux disease. The ill effects of Reglan use has not become fully apparent until recently. The FDA has announced that…
In November of 2009, Yaz and a similar product Ocella were recalled following reports of serious injury in users as young as thirteen years old. The problems associated with Yaz and Ocella involve the dosage of drospirenone which is known for creating health problems in users that live in European…
Prempro is subject to another cause for alarm because of a recent recall. This drug recall affects two lots of the product, namely Lot C83323 (exp. 3-10) and Lot D82196 (exp. 12-10). Nearly, 50,000 cartons of Prempro are included in this particular drug recall. Wyeth Pharmaceuticals, the manufacturer of Prempro,…
Roman Shades have been recalled by several companies over recent months following reports of strangulation in children the used the blind chords. Most recently, Ethan Allen joined the recall to include over 150,000 Roman Blinds. There were no reports of injury. However, all people using the Roman blinds should immediately…
Cardiac patients should be aware of the Class I Recall involving Thomas Medical Products with the company’s Transseptal Sheath Introducer Kit, also known as HeartSpan, CHANNEL FX, and Torflex, Braided Guiding Introducer Kit. This medical device is used in cardiac patients to pass a heart catheter from one side of…
Dialysis Systems by Baxter called HomeChoice and HomeChoice PRO are under a medical device recall following reports from physicians that people have experienced serious injury and one known death because of a defect in the product. The specific defect is unknown at this time. What is known is that the…
Millions of Becton, Dickinson and Company catheter systems are involved in a recall because of a defect in the product that may result in injury or death to a user. The direct flaw of the catheter system involves the risk of an air embolism and leakage of blood or therapeutic…