Colorado updates in category: Medical Malpractice

Imagine going to the hospital for a routine hernia operation. Imagine you wake up and find two incisions instead of one as expected because the surgeon operated on the wrong side and had to start over.Imagine getting your insurance statement a few weeks later and find your insurance had been billed for both operations!This is the true story of Kevin Baccam, a 33-year old school district...

USA Today recently reported that nursing home citations have increased 22% from 2000 to 2006. The U.S. Centers for Medicare and Medicaid Serices, which regulates nursing homes, claimed that more and more nursing homes are being cited for serious violations that are putting patients at risk. The most serious type of cases being cited are patients who were physically or sexually abused as well as...

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...

Defibrillator leads that connect an implanted defibrillator have been recalled. The defective medical device is made by Medtronic and may cause the device to function incorrectly. The name of the product is Medtronic Sprint Fidelis Defibrillator Leads. The FDA has advised patients who are implanted with this recalled Medtronic defibrillator lead or do not know the model of their lead, to...

A medical malpractice case is being heard in Arkansas after a woman was incapcitated after surgery at Northwest Medical Center. The case is being heard in Washington County Circuit Court. The woman had an infection in her arm and had surgery to treat it. The plaintiffs seek money either for expenses for their daughter's future costs at the nursing home or for her to stay at home with them....

A study being published in the New England Journal of Medicine found that most surgeons who have accidentally stuck themselves with needles while performing surgery, failed to report their injuries. This is a major problem because this lack of reporting is putting many patients and doctors at risk for blood-borne illnesses, such as AIDS and hepatitis.Most surgeons say the main reason for needle...

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...

Earlier this month a law firm out of Mt. Pleasant, South Carolina, announced that they are filing suit on behalf of their client against Davol, Inc., the manufacturer of Composix Kugel Mesh Patch, which as been used in a number of hernia repair surgeries. The defective medical device has been known to cause serious complications in patients who have undergone hernia surgery in which is was...

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...