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First introduced in 2003, the Medtronic Paradigm Insulin Pump 712 is a newer, upgraded version of the Medtronic MiniMed 722, a diabetes management device.

Paradigm Insulin Pumps, also known as MiniMed Insulin Pumps, deliver a steady, constant stream of insulin to diabetes patients, allowing them to:
The MiniMed system is, currently, the leading insulin pump therapy system prescribed in the U.S.
Some of the modernizations and improvements made to the Paradigm Insulin Pump 712 include a(n):
Currently, the newest version of the Paradigm 722 is the MiniMed Pump 715, which was first introduced in 2004 (on the heels of the 712 version).
Like the MiniMed Insulin Pump 722, the 712 version has a substantial reservoir that can hold up to 3 ml of insulin (or 300 units of insulin). This device is only recommended for diabetes patients who:
Defects in Lot 8 of Paradigm MiniMed Insulin Pumps have caused more than 200 hospitalizations due to the development of hyperglycemia, a life-threatening condition marked by extremely high blood glucose levels. Without treatment, hyperglycemia causes blindness, kidney disease and, eventually, death.
Due to mounting injury reports, in July 2009, Medtronic issued a voluntarily, Class I recall of defective infusion sets (components that are sold with insulin pumps and are used to implant a small tube beneath the skin). This nationwide recall affects the following model numbers:
Individuals in possession of recalled devices can receive a full refund by returning the pump to the place of purchase. If they have suffered an injury after using a Medtronic Paradigm Insulin Pump 712, it is important for them contact an experienced injury attorney for help. Injured parties will be able to obtain compensation for their injuries and losses, including financial, emotional and physical.
For more information or to discuss your concerns with an attorney for medical devices, please contact our MiniMed Insulin Pump Lawyers today.
Our injury and death lawyers are investigating all MiniMed cases. Our evaluations are not limited to persons injured by the recalled "Lot 8" infusion sets. To discuss the details of your unique circumstances, please contact our law offices today.
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