Physio-Control Issues Voluntary Field Action for LIFEPAK 1000 Defibrillators

A LIFEPAK 1000 defibrillator attorney notes that Physio-Control has announced a voluntary field action for the emergency defibrillators due to reported instances where the device has shut down unexpectedly during patient treatment. Defective devices may put patients at serious risk of harm or even death. Affected patients and their families may be eligible to pursue compensation with the help of a defective medical device lawyer.

For more information, contact Attorney Group today. We offer free, confidential, no obligation consultations. We can help answer your questions, and if you choose to pursue a case we can connect you with an affiliated LIFEPAK 1000 defibrillator attorney who can assist you throughout the legal process.

Important: The time you have to pursue a claim is limited. Contact us for more information.

Affected Defibrillators Could Shut Down Unexpectedly During Treatment

Physio-Control, manufacturer and distributor of emergency defibrillation equipment, announced that their LIFEPAK 1000 defibrillator may shut down unexpectedly due to an intermittent connection between the battery and the electrical contacts of the device. According to a press release issued through the U.S. Food and Drug Administration’s (FDA) recall alerts, the company has received 34 reports of devices shutting down during attempted use of the defibrillators. At the time of the press release, the company was aware of eight adverse events related to the issue.

The intermittent connection may be caused by wear and subsequent oxidation formation that has occurred over time in devices that have been exposed to vibration and batteries installed for long periods of time. Affected defibrillators may not be able to deliver therapy during a resuscitation attempt, putting patients at risk for serious harm or death. Physio-Control is contacting customers directly and advising them to remove and reinstall the battery in their devices. Additional information regarding the voluntary field action can be found here.

How a LIFEPAK 1000 Defibrillator Attorney Can Help

Medical device makers have a duty to provide safe products. If there are risks of harm associated with their devices, they also must provide adequate warnings. If a device maker fails to fulfill this duty, it could be held liable in lawsuits for injuries that may result.

People injured by a defective emergency defibrillator may be eligible to recover money for:

  • Medical Expenses
  • Lost Wages
  • Pain and Suffering

The families of those killed may be eligible to recover money for funeral expenses and the pain that comes with losing a loved one.

The Time You Have to Pursue a Claim is Limited. Contact Us Today.

For more information, contact Attorney Group. You can fill out the form on this page or contact us by phone or email.

After you contact us, an attorney will follow up to answer questions that you might have. There is no cost or obligation to speak with us, and any information you provide will be kept confidential.

Please note that the law limits the time you have to pursue a claim or file a lawsuit for an injury. If you think you have a case, you should not delay taking action.