FDA MedWatch - Medtronic Expands Recall of MiniMed 600 Series Insulin Pumps for Incorrect Insulin Dosing - Healthy Food Deals

If your email program has trouble displaying this email, view as a webpage. MedWatch - The FDA Safety Information and Adverse Event Reporting Program 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. Questions? If you have questions about this recall update, contact Medtronic's 24-Hour Technical Support line at 1-877-585-0166.   Read More

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