Ennis & Ennis, P.A. Blog: FDA Recalls Certain Medtronic SynchroMed II Infusion Pumps

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Ennis & Ennis, P.A. Blog: FDA Recalls Certain Medtronic SynchroMed II Infusion Pumps

FDA Recalls Certain Medtronic SynchroMed II Infusion Pumps

- Beckers

09/26/2011 - The FDA has ordered a recall of Medtronic's SynchroMed II implantable infusion pump, models 8637-20 and 8637-40, distributed between May 2004 and July 8, 2011, according to an FDA news release.

The devices may have reduced performance due to formation of a film within the pump battery. This problem can lead to the sudden loss of therapy and the return of underlying symptoms or therapy withdrawal symptoms.

Medtronic began notifying physicians with an Urgent Medical Device Correction letter beginning July 5, 2011. The company has a device identification website where customers can enter the serial number of their SynchroMed II infusion pump to find out if it is being recalled.

More Medtronic SynchroMed II Pain Infusion Pump Recall Lawsuit News::

If you have experienced Medtronic SynchroMed II side effects you may be entitled to compensation. Contact the Medtronic Infusion Pain Pump lawyers of Ennis & Ennis, P.A. today for information regarding your potential drug infusion pump lawsuit or for information about a possible Medtronic SynchroMed II class action lawsuit. Fill out our free case evaluation form and our on-staff nurse or one of our Attorneys will contact you regarding your potential Medtronic SynchroMed II case. Fill out our online case evaluation form or call us toll free at: 1.800.856.6405 for your free, confidential case evaluation.

Medtronic SynchroMed II Infusion Pump Recall Information::