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Potential Medtronic Infusion Pump Malfunction Claims: Resource4thePeople Attorneys Now Providing Consulations
Date:10/21/2013

San Diego, CA (PRWEB) October 21, 2013

http://www.resource4thepeople.com/defectivemedicaldevices/medtronic.html#sthash.BtTyiPoe.dpuf

Resource4thePeople announced today that its national network of lawyers are now reviewing allegations from consumers who may have suffered health problems as a result of Medtronic Infusion Pumps that were the subject of a recall by the Food and Drug Administration.

The FDA in a June 3, 2013 Class 1 Recall Notice* alerted health care professionals and consumers that electric shorting problems had been identified in the Medtronic SynchroMed II and SynchroMed EL Implantable Drug Infusion Pumps.

In its notice, The FDA said the pumps contain and administer prescribed drugs to a specific site inside the patient’s body. Currently, the approved drugs for use with the SynchroMed Infusion Pump are Infumorph, Lioresal, Prialt (Ziconotide), Floxuridine, Methotrexate and Gablofen. The SynchroMed pumps are used to treat primary or metastatic cancer, chronic pain, and severe spasticity.

"The FDA said that in instances in which the problems that generated the recall occurred patients may have been placed in life-threatening situations," said Resource4thePeople.

"In response to the numerous inquiries we have been receiving from consumers over these recalls were are now reviewing allegations of health problems and offering free consultations about legal options that may be available to seek compensation for those who may have been injured."

The FDA describes Class 1 recalls as the most serious type of recall and involve situations in which there is a reasonable probability that use of these products will cause serious adverse health consequences or death.

The FDA listed this Reason for Recal
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