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The MiniMed insulin pump therapy system is a diabetes management device that continuously delivers fast-acting insulin to diabetics. Produced by Medtronic since 1983, the MiniMed system includes a(n):

Currently, the Medtronic MiniMed pump is the leading insulin pump therapy system prescribed in the U.S.
Despite the number of components associated with the MiniMed, these insulin pumps are easy to use and, purportedly, deliver more precise amounts of insulin than syringes. To properly use the MiniMed REAL-Time System:
To minimize complications with this device it's essential to regularly check:
Defects with the Quick-set Infusion set, the device that implants the cannula subcutaneously, led Medtronic to voluntarily issue a nationwide recall in July 2009. While only 60,000 sets are suspected to be defective, over 3 million sets with the following model numbers have been pulled off the market:
This recall is a Class I recall, the most serious classification for recalls.
Individuals in possession of recalled devices should return the device to the place of purchase for a full refund.
Use of defective infusion sets has, to date, caused more than 200 diabetics to be hospitalized due to hyperglycemia, dangerously high blood sugar that can cause:
Have you or a loved one been injured after using a Medtronic MiniMed Insulin Pump System? If so, contact us today to consult with an experienced MiniMed Insulin Pump Lawyer who will evaluate your case and help you recover a monetary award for your losses.
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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