Medtronic, the largest seller of heart rhythm medical devices in the world, has warned that 37,000 of its Sigma and Kappa heart pacemakers implanted since 1997 may be wired incorrectly. At least two deaths may be linked to the defective products.

Defective pacemakers

Medtronic has reported that approximately 37,000 of its Sigma and Kappa pacemakers implanted since 1997 may have wiring problems that could cause the pacemakers to fail at a higher than expected rate. The company says that wiring separation issues, along with the use of cleaning solutions during the manufacturing process, may be the cause for the potential defects. The company recently advised doctors of these issues. To see what was sent, please click here.

Product liability, wrongful death and whistleblower lawsuits pending

Problems with Medtronic’s pacemakers are just the latest in a series of troubles for the medical device giant. Following the recall of its Sprint Fidelis defibrillators in 2007, the company has also been linked to corrupt practices concerning the marketing of some of its products – most notably its Infuse Bone Graft product. Product liability, wrongful death and whistleblower lawsuits have been filed against the company – the latter involving a former employee who says that Medtronic paid doctors to use its products in ways not approved by the U.S. Food & Drug Administration (FDA).

More troubles for Medtronic

Lawsuits filed against the company are only part of Medtronic’s troubles. News agencies are reporting that the company will terminate as many as 1,800 workers and that its stock has taken a turn for the worst. While some of that may have to do with the economy, the continuous scandals, recalls and lawsuits almost certainly don’t help.

If you’ve been injured by one of Medtronic’s products, contact an experienced products liability attorney to discuss your situation – even if it’s just to evaluate your options. If you’ve been injured, you may be entitled to money damages.