Medtronic Pain Pump Linked to Dosing Errors, Deaths. Medtronic Pain Pump Linked to Dosing Errors, Deaths . Medtronic PLC is facing scrutiny over its SynchroMe

Filing a Lawsuit for Medtronic Insulin Pump Injuries. If you or a loved one has suffered due to the malfunction of a Medtronic insulin pump, you may have the right to file a product liability lawsuit. These lawsuits hold manufacturers accountable for …

Filing a Lawsuit for Injuries Linked to MiniMed 600 and 700 Series Pump Failures. In October 2024, Medtronic issued an urgent recall notice for its MiniMed 600 and 700 series insulin pumps, notifying users of a potential defect leading to shorter battery life.

The Food and Drug Administration has issued a warning letter and requested a meeting with officials from Medtronic Inc. regarding its defective SynchroMed II drug infusion pump. These infusion pumps are used to deliver painkiller and other drugs into patients on a regular or prolonged basis. The SynchroMed II is approved to deliver morphine sulfate, […]

A number of lawsuits were recently brought against device maker. A number of lawsuits were recently brought against device maker, St. Jude Medical.

Device maker, Medtronic Inc, just wrote to physicians about potential reduced battery problems with its SynchroMed II Implantable Drug Infusion Pumps. Reuters noted that, as of May 31, 55 confirmed cases of battery reduction problems were received globally. About 139,653 devices have been implanted around the world. The issue does not affect Medtronic’s external insulin […]

Medtronic Inc. has received a warning letter regarding its SynchroMed II Drug Pumps and MiniMed Paradigm Insulin Pump. In the letter, the Food & Administration (FDA), cites Medtronic for taking too long to recall the SynchroMed pumps. The letter also said that an inspection conducted last year at the Puerto…

Medtronic Inc. has issued a Class I recall for the SynchroMed II Programmable Pump, SynchroMed EL Infusion System and Refill Kits. These defective medical devices have been linked to 8 deaths. The SynchroMed II Programmable Pump and the SynchroMed EL Infusion System are used in patients undergoing therapy that requires…

Device maker giant, Medtronic, Inc., just announced that it received a warning letter from the U.S. Food & Drug Administration (FDA). According to the Twin Cities Business Journal, the letter came after an inspection of Medtronic’s Mounds View Cardiac Rhythm Disease Management site and concerned: “Corrective and preventative action and field-action timeliness, review and ...

Medtronic has announced that the U.S. Food and Drug Administration (FDA) has classified two global voluntary recalls of HeartWare International’s HeartWare Vent