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Medtronic, a medical device manufacturer based in Northridge, CA, has been manufacturing different versions of the Paradigm MiniMed insulin pump therapy system since 1983. While the Medtronic MiniMed pumps were first introduced in the 722 and 522 series, since then, modernized versions have included:

The primary difference between the 7xx versus the 5xx versions of the MiniMed insulin pump is that the reservoir in the 7xx can hold nearly three times as much insulin as the 5xx's reservoir. As a result, the 7xx version of the Paradigm insulin pump is generally recommended for diabetes patients who:
The components necessary to proper functioning of the insulin pump include:
Because insulin pump therapy systems can vary the amount of insulin they administer (according to a patient's changing needs), they have significantly improved diabetes management (when they work properly).
The Medtronic Paradigm MiniMed pump is only available via prescription. However, it is distributed by a number of pharmacies – physical stores and online sites – available nationwide.
For insurance purposes, most MiniMed insulin pump distributors sell each component of insulin pump therapy systems separately.
In July 2009, Medtronic announced that:
Classified as a Class I Recall, this MiniMed insulin pump recall affected units nationwide and, according to the FDA, has caused more than 200 hospitalizations to date.
Diabetes patients who sustain serious injuries, such as hyperglycemia, following use of defective insulin pump systems will have a legal claim against Medtronic, entitling them to seek compensation for their medical bills, lost wages and pain and suffering.
For more information, contact 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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