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Medtronic Expands Recall of MiniMed Insulin Pumps for Incorrect Insulin Dosing

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Serious injuries or death may result from the use of these devices. The FDA has identified this as a Class I recall, the most serious type o

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FDA - Center for Devices and Radiological Health

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Medtronic Expands Recall of MiniMed 600 Series Insulin Pumps for Incorrect Insulin Dosing

On October 5, 2021, Medtronic expanded and updated its 2019 recall of MiniMed™ 600 series insulin pumps to include replace any MiniMed™ 600 series pump that has a clear retainer ring at no charge to customers.

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.

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Questions?

If you have questions about this recall update, contact Medtronic's 24-Hour Technical Support line at 1-877-585-0166.  


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