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MiniMed600 Insulin Pump Recall

The FDA has issued a Class I recall of some of the Medtronic MiniMed600 insulin pumps.

This is the most serious kind of recall, because of a potentially fatal risk of incorrect dosing.

The specific models are Model 630G (distributed September 2016 to October 2019) and Model 670G (June 2017 to August 2019).

If you are a supplier, please immediately alert all Medicare beneficiaries that have received one of these pumps from you.

If you are a Medicare beneficiary, please contact your health care provider immediately.


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