CareFusion Infusion Pump Recall Lawsuit
FDA Gives Highest Priority to CareFusion Recall
October 19, 2010 – The FDA has assigned its most serious classification to an August 2010 recall of CareFusion Alaris PC 8015 electronic intravenous infusion pumps. According to the company, a glitch that causes the device to freeze could cause “… serious adverse health consequences or death.”
CareFusion says certain wireless network conditions can cause intermittent communication errors that freeze the unit’s display screen. The devices being recalled were manufactured between December 2008 and September 2009.
Do I have a CareFusion Injury Lawsuit?
The Products Liability Litigation Group at our law firm is an experienced team of trial lawyers that focus on the representation of plaintiffs in CareFusion infusion pump injury accident lawsuits. We are handling individual litigation nationwide and currently accepting new cases in all 50 states.
Free Care Fusion Infusion Pump Recall Case Evaluation: If you or a loved one has been injured or suffered adverse side effects after using an infusion pump included in this recall, you should contact our law firm immediately. You may be entitled to compensation by filing a lawsuit and we can help.
To contact us for a free review of your potential case, please fill out the form below or call us toll free 24 hrs/day by dialing: (866) 588-0600.
