{"url_path":"/fda/device/recalls/Z-2981-2026","section_key":"summary","section_title":"DEVICE Recall: Medtronic MiniMed, Inc. — MiniMed 670G Insulin Pump, Model: MMT-1781, MMT-1782;","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-2981-2026%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":105,"has_tables":false,"body_markdown":"# FDA DEVICE Recall: Z-2981-2026\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 670G Insulin Pump, Model: MMT-1781, MMT-1782;\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-1781/00763000404536/NG2665223H, NG2748200H, NG2748664H, NG2755237H, NG2716176H, NG3547582H.  MMT-1782/00763000404543/NG2768190H\n\n## Distribution\nInternational distribution to the countries of Germany, Denmark, Austria, Netherlands, United Kingdom, Italy, Belgium, Ireland, Switzerland, Sweden, Northern Ireland."}