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Medtronic MiniMed 600 Series Insulin Pump Lawsuits

The MiniMed insulin pump is used to deliver insulin to people with Type 1 diabetes. Medtronic, the manufacturer of the MiniMed Insulin Pump Model 630G (for persons 16 years of age and older) and Model 670G (for persons seven years of age and older), issued an urgent recall because of a defective or missing retainer ring that may cause either too much too or too little insulin to be delivered to the patient.

Medtronic MiniMed 600 Series Insulin Pump Lawyers are Ready to Help

Contact our Medtronic MiniMed 600 Series Insulin Pump Lawyers to review whether you or a family member may be entitled to financial compensation. Levy Konigsberg LLP is currently accepting Medtronic MiniMed 600 Series Insulin Pump cases in all 50 states.

If you or a loved one has suffered one or more of these complications, you may be entitled to a cash award and compensation for medical expenses. For a free confidential consultation with Medtronic MiniMed 600 Series Insulin Pump Lawyers at our law firm, please call (800) 315-3806or submit an email inquiry.

What is Medtronic MiniMed 600 Series Insulin Pump?

Medtronic’s MiniMed 600 Series Insulin Pump Systems provide automated insulin delivery for better management of Type 1 diabetes. The technology mimics the function of a normal pancreas by supplying insulin as needed and avoiding dangerous fluctuations in the patient’s insulin levels.

What is Happening with Medtronic MiniMed 600 Series Insulin Pump?

Medtronic announced a recall of its MiniMed 600 Series Insulin Pumps due to the presence of a defective retainer ring. The damaged retainer ring cannot securely hold the insulin cartridge in place. This may result in the pump delivering a dose of insulin that is different than the dose prescribed to the patient. An incorrect insulin dosage can lead to hypoglycemia or hyperglycemia. Severe hyperglycemia can cause a loss of consciousness, seizure, or death. Medtronic has received 2,175 reports of injuries and one reported death associated with this defect.

The U.S. Food and Drug Administration (FDA) has labeled this action a Class I recall, which is the most serious type of recall issued by the FDA. The FDA warns that using MiniMed 600 Series Insulin Pumps can result in serious injuries or death.

https://www.fda.gov/medical-devices/medical-device-recalls/medtronic-recalls-minimed-insulin-pumps-incorrect-insulin-dosing

Medtronic MiniMed 600 Series Insulin Pump Side Effects and Complications

Complications of Medtronic MiniMed 600 Series Insulin Pumps include:

  • Hypoglycemia (a decrease in glucose below normal levels);
  • Hyperglycemia (an increase in glucose above normal levels);
  • Loss of consciousness;
  • Seizure; and
  • Death.

Medtronic MiniMed 600 Series Insulin Pump Lawyers are Ready to Help

Contact our Medtronic MiniMed 600 Series Insulin Pump Lawyers to review whether you or a family member may be entitled to financial compensation. Levy Konigsberg LLP is currently accepting Medtronic MiniMed 600 Series Insulin Pump cases in all 50 states.

If you or a loved one has suffered one or more of these complications, you may be entitled to a cash award and compensation for medical expenses. For a free confidential consultation with Medtronic MiniMed 600 Series Insulin Pump Lawyers at our law firm, please call (800) 315-3806or submit an email inquiry.

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