MiniMed 600 Series Class I Recall | Tech Thursday

Medtronic has recalled certain MiniMed 600 Series insulin pumps for delivering incorrect insulin dosing. Medtronic has recalled the following pump models:

Model 630G distributed Sept 2016 to Oct 2019
Model 670G distributed June 2017 to Aug 2019

The FDA has identified this as a Class I recall, the most serious type of recall.  Use of these devices may cause serious injuries or death.

Reason for Recall

Medtronic is recalling the specified insulin pumps due to a missing or broken retainer ring which helps to lock the insulin cartridge into place in the pump’s reservoir compartment.

If the cartridge is not locked firmly into place, under or over the delivery of insulin may occur, which could result in hypoglycemia or hyperglycemia. Severe hyperglycemia can result in a loss of consciousness, seizure, and death.

The firm has received a total of 26,421 complaints in which the device malfunctioned in this manner. The firm is aware of 2,175 injuries and 1 death.

Contact Information

Customers who have questions or need additional information or support about this recall should call the 24-hour Medtronic Technical Support at 877-585-0166.

For more information, please see this FDA Info Sheet

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