Medical Malpractice | InjuryBoard Denver

Recently, researchers found that only half of all U.S. doctors report medical mistakes or unethical colleagues. Only 46 percent of physicians surveyed stated that they knew of a serious medical error and didn't report it. The U.S. Institute of Medicine surveyed more than 1,600 physicians in 2003 and 2004; only 31 percents had undergone a competency review in the past three years. About 98,000...

Numerous hospice providers nationwide are facing financial problems due to their patients living longer than expected. You would assume this would obviously be a positive development, yet the effects on hospices' aren't.Over the last eight years, the federal government has had to demand that hospices exceeding reimbursement limits repay hundreds of millions of dollars to Medicare.A 2006 report...

Some flow generators used in the treatment of sleep apnea have been recalled. ResMed is voluntarily recalling S8 flow generators made between July 2004 and May 15, 2006 because the power supply connector may short circuit. This creates a potential for machine failure, sparks and fire. Patients may continue to use their S8 flow generators until they receive a replacement device. As with any...

An interesting article in The Denver Post yesterday addresses administrative problems in hospitals that could be to the detriment of health care workers and patients, possilby leading to medical malpractice.The article tells the story of a hospital cleaning crew supervisor who was fired after repeatedly asking for more staff members to help them do a better job. Nurses and others complained that...

Defibrillator manufacturer Medtronic asked the US District Court of Minnesota to consider a motion for summary judgement. Their request was based on the claim that federal preemption barred the plaintiffs' claims. The plaintiffs' main complaint sites state law product liability claims sounding in negligence and strict liability. Other claims include violations of state Consumer Protection...

According to Medtronic's website, "Medtronic is the global leader in medical technology - alleviating pain, restoring health and extending life for millions of people around the world." Medtronic manufactures cardiac resynchronization therapy defibrillators (CRT-D's) and implantable cardioverter-defibrillators (ICD's). These devices are used on patients with heart conditions and are surgically...

On September 29, 2006, The Heart Rhythm Society (HRS) finalized recommendations for revising the system used by industry, regulators and clinicians to monitor and publicize implantable-device performance problems. Key goals of the recommendations include:• improved recognition of potential device malfunctions• postmarket surveillance and reporting of any problems• communication among...

The FDA issued a warning to Medtronic, Inc. on Friday, September 29, 2006 regarding the delayed filing of a post market surveillance interim report on the AneuRx Stent Graft System. According to Medtronic, Inc. the letter is not related to the quality, design or manufacture of the product. However, the purpose of the Postmarket study is to make sure the device is appropriately labeled for use...

About 85,000 Taxus stents are being recalled voluntarily by Boston Scientific because of possible defects. Of the 42 complaints received, 30 systems showed actual performance flaws generally thought to be the result of excess heat being applied during the laser welding stage during the manufacture of the product; 200 Taxus stents were recalled earlier this month. In a meeting with the FDA in...

The US Food and Drug Administration (FDA) and MRL, Inc (a Welch Allyn company), recently notified healthcare professionals about the class 1 recall of 1184 automated external defibrillators ([AEDs] Welch Allyn PIC 50, catalog #97108X) manufactured during February 2002 to October 2004; 673 units were sold within the United States.The recall occured because of an electrical contact problem that...

The FDA's prime responsibility is to insure that the public is protected from unsafe drugs and medical devices. Recent studies suggest that the FDA is falling well short of it's goal. Even more surprising, these concerns have been raised from within the FDA itself.Today, the Union of Concerned Scientists released a survey noting that more than a third of FDA scientists said agency officials...

Pharmacists and physicians belong to two of the most trusted professions in America. We routinely follow our doctors advice regarding drugs they prescribe and then trust that our pharmacists will correctly fill the order. Unfortunately, many times our trust is misplaced. Today the Institute of Medicine released a report noting that medication errors harm 1.5 million people each year. The...

MRL, Inc. and FDA notified healthcare professionals of a voluntary worldwide Class I recall of 580 AED20 automatic external defibrillators because of an intermittent electrical connection that could result in failure, delay in analyzing the patient's ECG or failure to deliver expected therapy and resuscitation of the patient. A Class 1 recall occurs when there is reasonable probability that use...

I read a story today about a Tacoma physician filing a medical malpractice lawsuit involving his wife's recent death. While you cannot make a good determination based on just what you read in the papers, it appears as if her death should have been prevented. We, of course, sympathize with the family and offer our condolences.Medical malpractice damage caps affect us all. I hope our legislators...

Many of you have learned of recent problems associated with implantable cardiac devices. Guidant Corporation's implantable defibrillator has been associated with potentially fatal complications. As a result of negative publicity, Guidant created a panel to investigate complaints. The May 18 edition of the New England Journal of Medicine contains an early release of their findings. Of note,...