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Product Recalls & Refunds Online / National

Medtronic MiniMed, Inc.: MiniMed 780G Insulin Pump, , MMT-1886, MMT-1895,

Reward FDA device recall — free correction, repair, or replacement from manufacturer or authorized retailer

Recall reason: A software anomaly can occur when the pump is paired with the Instinct sensor. Under certain circumstances, the pump unexpectedly stops delivering insulin and displays two error messages back-to-back: Pump Error 53 followed immediately by Pump Error 23. Insulin delivery will stop which may lead to delayed therapy and an increased risk of hyperglycemia or diabetic ketoacidosis (DKA).. Recalled by Medtronic MiniMed, Inc.. Distribution: International distribution to the countries of Spain, Great Britain, Netherlands, Italy.. Classification (Class II — potential health risk). Affected lots/dates: UDI-DI/GTIN: A7630006392701, 00763000521554, 00763000639273, A7630006392301, 0019915

Reward FDA device recall — free correction, repair, or replacement from manufacturer or authorized retailer
Category Product Recalls & Refunds
Location National
Eligibility U.S. consumers who own or purchased the recalled medical device. Contact the manufacturer or the retailer/pharmacy where you purchased it to arrange for a free correction, repair, or replacement. Have the model number ready if possible.
Source Official Source ↗
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