Two More Die From Malfunction In Medtronic Drug Pump
Nov 2, 2016. Two More Die From Malfunction In Medtronic Drug Pump Device. implantable drug pump device, which has been recalled three times in recent years. been implanted in patients going through intrathecal baclofen therapy. Apr 27, 2015. Medtronic ordered to stop most sales of drug pump. The FDA later classified that communication as a Class I recall, which is the most critical. Sep 13, 2011. The Medtronic SynchroMed II Implantable Infusion Pump recall affects. In some cases, like with patients receiving intrathecal baclofen to treat.
FDA deal sharply limits Medtronic infusion pump
May 22, 2015. Unfortunately, these devices have been recalled several times after they were linked to. SynchroMed Pain Pumps and Baclofen Withdrawal. Apr 20, 2012. Last year, Medtronic issued two Class I recalls of its SynchroMed Drug Infusion Pumps, a line of products that had been recalled for defects. May 15, 2015. plantation of a baclofen pump device does not come with- out risks. Medtronic, Inc. did recall a large number of SynchroMed pumps due to a.
Medtronic SynchroMed Infusion Pump Lawsuit Pain
August 2007 – Class I Recall issued for the Medtronic SynchroMed El Implantable Infusion Pump. The devices, which are part of the SynchroMed EL Infusion. Medtronic's SynchroMed II & EL Implantable Infusion Pumps may cause deadly. FDA approval for injecting morphine, ziconotide, Lioresal baclofen, floxuridine. the FDA classified Medtronic's label changes as a Class I recall, meaning the.