If you or someone you know has a Medtronic implantable medicine pump, it is important to know about a recent Complaint Filed by the U.S. Attorney’s Office in regards to manufacturing problems. This injunction filed April 27, 2015 against Medtronic and its CEO, seeks to prevent them from selling SynchroMeds that have been adulterated and to force them to improve the quality of their manufacturing methods. It describes numerous violations of the quality system regulations at Medtronic Neuro and states that many of the violations related directly to the manufacture of the SynchroMed II implantable infusion pump. The complaint references four inspections where the FDA observed and documented violations.
If your SynchroMed pump is not functioning correctly or if you had your implant removed due to problems, please call or email our office to see if you can recover damages.
The Meyerson Law Firm, P.C. (512) 330-9001
