MiniMed Insulin Pump

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Medtronic Paradigm Insulin Pumps

Known by the brand name MiniMed, the Medtronic paradigm pumps are insulin management devices that, when worn 24/7:

provide a continuous flow of insulin to diabetics
use a glucose sensor to alter the amounts of insulin administered, according to an individual's changing needs
give diabetics more freedom in their eating and exercise schedule
eliminate the need for multiple daily injections

Here is a description of the Medtronic MiniMed Paradigm pump system and its parts:

The Quick-set infusion set, a disposable device, implants a small tube (cannula) beneath the skin in a minimally painless manner
The REAL-Time insulin pump connects to the cannula and delivers the appropriate amount of insulin

Because insulin pumps should be worn constantly, it's recommended that diabetics place these devices in their pockets or on their waist bands.

Problems with Paradigm Pumps by Medtronic

Despite its success at managing diabetes, some MiniMed pumps have been reported to cause severe health problems due to defects in the device. Currently, over 200 diabetics have undergone hospital treatments due to:

bends in the cannula that were impeding insulin flow
a disconnect between the cannula and skin or the cannula and pump that stopped insulin flow
defects in the glucose sensor that cause excessive amounts of insulin to be delivered

Life-threatening health complications caused by these defects include (but aren't limited to):

hyperglycemia , extremely high blood sugar levels that, if left untreated, can cause blindness, heart disease, kidney disease and death
diabetic ketoacidosis , a condition in which extremely low levels of blood sugar cause the body to break down its own fats and produce toxic ketone acids

If left untreated, diabetic ketoacidosis can result in hypokalemia (dangerously low levels of potassium in the blood), brain swelling and death.

Medtronic Minimed Insulin Pump Recall

Due to mounting patient reports regarding injuries from Medtronic insulin pumps, on July 10, 2009, Medtronic issued a voluntary, national recall of the following Quick-set systems:

MMT-359S6
MMT-359S9
MMT-359L6
MMT-359L9

While about 60,000 infusion sets are suspected to be defective, a total of 3 million have been pulled off the market, and individuals who have returned these products have been issued a full refund. This Medtronic MiniMed recall has been classified as a Class I recall, the most serious type of recall that can be issued by the FDA or a manufacturer.

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 Lawyers who will evaluate your case and help you obtain the settlement you deserve.

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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