{"url_path":"/fda/device/recalls/Z-2980-2026","section_key":"summary","section_title":"DEVICE Recall: Medtronic MiniMed, Inc. — MiniMed 640G Insulin Pump, Model: MMT-1711, MMT-1712;","topic":"fda","document":{"doc_type":"device-recall","doc_date":"2026-07-13","source_url":"https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2980-2026%22","accession_number":null,"cik":null,"ticker":null,"issuer_name":null,"edgar_url":null,"primary_entity_key":null,"primary_entity_name":"Medtronic MiniMed, Inc."},"word_count":113,"has_tables":false,"body_markdown":"# FDA DEVICE Recall: Z-2980-2026\n\n**Recalling firm:** Medtronic MiniMed, Inc.\n**Classification:** Class II\n**Status:** Ongoing\n**Type:** Voluntary: Firm initiated\n**Initiated:** 2026-07-13\n**Report date:** 2026-08-26\n\n## Product\nMiniMed 640G Insulin Pump, Model: MMT-1711, MMT-1712;\n\n## Reason\nLoaner 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.\n\n## Affected lots\nModel/UDI-DI/Serial Numbers: MMT-1711/00763000404550/NG2660048H, NG2663343H, NG3015306H;  MMT-1712/00763000404567/NG2628486H, NG2758213H, NG2999651H, NG3349198H, NG3351719H, NG2678842H, NG2831821H, NG2831546H, NG2932027H, NG3049657H, NG3033094H, NG2831538H, NG3738739H\n\n## Distribution\nInternational distribution to the countries of Germany, Denmark, Austria, Netherlands, United Kingdom, Italy, Belgium, Ireland, Switzerland, Sweden, Northern Ireland."}