Medtronic MiniMed, Inc.
What this record is not
A recall record is reproduced as FDA published it, and the classification is FDA’s. SPEQ adds no interpretation, and a recall concerns the products and dates in the record — it is not a statement about a company’s other products or its current status.
Loaner insulin pumps may have been cleaned with chemically incompatible products that could damage the pump case or keypad, allow moisture ingress, and result in insulin over- or under-delivery, potentially causing hypoglycemia, hyperglycemia, or diabetic ketoacidosis.
MiniMed 670G Insulin Pump, Model: MMT-1781, MMT-1782;
Model/UDI-DI Serial Numbers: MMT-1781/00763000404536/NG2665223H, NG2748200H, NG2748664H, NG2755237H, NG2716176H, NG3547582H. MMT-1782/00763000404543/NG2768190H
Data: U.S. FDA. Recall details are as reported by the FDA. The quality-domain mapping and severity are a SPEQ editorial interpretation of the recall reason, not an official FDA classification. Open the enforcement explorer →