MiniMed® 670G MMT-1780KPK (UDI 00763000190460)Recalls & reported problems

Summary

The FDA's MAUDE database contains 33,713 adverse event reports that list this exact device (DI 00763000190460), received between Oct 2, 2018 and Jul 7, 2025 — classified as 51 deaths, 9,759 injuries, 23,903 malfunctions.

The most frequently reported specific device problem is “Patient Device Interaction Problem” (11,310 reports).

2 FDA recall records name this device's identifier, 2 still open.

12 other recalls cover devices cleared under the same FDA submission (P160017); they may or may not involve this specific model.

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.

Recalls naming this device

1. Feb 13, 2026Class IIOpen, Classified

   All Medtronic MiniMed infusion pumps (Paradigm series, 600 series, and BLE 700 series) were found to be affected by unintended over- and under-delivery of insulin when the pump is elevated or lowered relative to the infusion site, respectively, because of changes in gravitational force impacting hydrostatic and hydrodynamic pressures. Insulin over-delivery, which can occur when the pump is elevated relative to the infusion site, can result in severe hypoglycemia, altered mental status, seizure, coma, or death. An under-delivery of insulin, which can occur at lowered pump height conditions relative to the infusion site, can result in severe hyperglycemia, dehydration, diabetic ketoacidosis, or death.

   Z-1739-2026 · Root cause: Device Design · Recall details · FDA record ↗

2. Jul 31, 2024Class IOpen, Classified

   Insulin pumps that have been dropped, bumped, or experienced physical impact may have damage to internal electrical components, which may cause reduced pump battery life. Since the defect reduces the battery life overall, it shortens the time between low battery alarms and increases the frequency with which the user must insert a new battery. Further, the defect may also deliver the low battery alarm when there is significantly less time before the battery completely runs out, from the expected up to 10-hour buffer the low alert is supposed to signal, leading to device powering down and stopping insulin delivery unexpectedly. Per the firm, a subset of pumps with the defect showed the low alert alarm was delivered ~2.5 hours before the device shut off, however, patient reports indicate the time could be even shorter. Replacing the battery will not resolve this issue and the short battery life and the truncated low battery alert lead time will continue to occur. Early battery depletion could result in power loss and insulin delivery could be interrupted, resulting in under delivery of insulin potentially leading to hyperglycemia and/or DKA.

   Z-0003-2025 · Root cause: Device Design · Recall details · FDA record ↗

Most reported problems

Recent adverse event reports

The 25 most recent of 33,713 reports, in the reporter's own words as published by the FDA.

• MalfunctionJul 7, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED TO MEDTRONIC MINIMED THAT THE CUSTOMER EXPERIENCED HYPERGLYCEMIA. THE CUSTOMER ALSO REPORTED SENSOR UPDATING ALERT AND STATED THAT THE HIGH BLOOD GLUCOSE EVENT OCCURRED DURING THE FLIGHT. THE CUSTOMER WAS TREATED WITH AN INSULIN PUMP. THE EVENT INVOLVED PRODUCT(S) MMT-1780KPK. TROUBLESHOOTING WAS PERFORMED, WHICH INCLUDED EXPLAINING POSSIBLE CAUSES OF SENSOR UPDATING ALERTS, INSPECTING THE SENSOR TO ENSURE IT WAS SECURELY TAPED, AND ADVISING THE CUSTOMER ABOUT SENSOR PLACEMENT AND BEST PRACTICES FOR INSERTION WHILE STANDING UP. THE CUSTOMER DECLINED FURTHER TROUBLESHOOTING, INCLUDING TESTING THE TRANSMITTER OR REVIEWING SITE SELECTION, TAPING, AND CALIBRATION PROTOCOL. NO FURTHER PATIENT COMPLICATIONS WERE REPORTED. NO PRODUCT RETURN IS REQUIRED FOR MMT-1780KPK.

  Patient problems: Hyperglycemia

  MAUDE report 22409609 ↗
• MalfunctionJul 7, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED TO MEDTRONIC MINIMED THAT THE CUSTOMER EXPERIENCED LOW BLOOD GLUCOSE LEVELS AFTER FLIGHTS. THE CUSTOMER REPORTED NO ADVERSE EVENT. THE EVENT INVOLVED PRODUCT(S) MMT-1780KPK. TROUBLESHOOTING WAS PERFORMED BUT IT WAS UNKNOWN WHETHER THE INSULIN PUMP WAS UTILIZED WITHIN 48 HOURS OF THE EVENT ALSO, IT WAS UNKNOWN WHETHER THE AUTO MODE FEATURE WAS ACTIVE OR NOT. NO HARM REQUIRING MEDICAL INTERVENTION WAS REPORTED. THE PRODUCT WAS NOT RETURNED FOR ANALYSIS.

  Patient problems: Hypoglycemia

  MAUDE report 22409607 ↗
• MalfunctionJul 7, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED TO MEDTRONIC MINIMED THAT THE CUSTOMER EXPERIENCED HYPERGLYCEMIA DURING AIR TRAVEL, WITH BLOOD GLUCOSE VALUES REACHING 300 MG/DL. BLOOD GLUCOSE VALUE AT THE TIME OF THE EVENT WAS 300 MG/DL. THE CUSTOMER WAS TREATED WITH INSULIN PEN. THE EVENT INVOLVED PRODUCT(S) MMT-1780KPK, MMT-332A, AND MMT-943. TROUBLESHOOTING WAS PERFORMED, WHICH INCLUDED VERIFYING PUMP SETTINGS, INSPECTING TUBING AND RESERVOIR FOR LEAKS OR AIR BUBBLES, CHECKING THE INFUSION SET AND INSULIN VIAL, AND REVIEWING AUTO MODE OPERATION AND BOLUS DELIVERY PROCESSES. NO FURTHER PATIENT COMPLICATIONS WERE REPORTED. NO PRODUCT RETURN IS REQUIRED FOR MMT-1780KPK, MMT-332A, AND MMT-943.

  Patient problems: Hyperglycemia

  MAUDE report 22409600 ↗
• MalfunctionJun 25, 2025Battery Problem; Battery Problem

  IT WAS REPORTED TO MEDTRONIC MINIMED THAT THE CUSTOMER EXPERIENCED HYPERGLYCEMIA. THE CUSTOMER ALSO REPORTED RAPID BATTERY DEPLETION AND RECURRING "REPLACE BATTERY" ALERTS. THE CUSTOMER WAS TREATED WITH MANUAL INJECTION. THE EVENT INVOLVED PRODUCT(S) MMT-1780KPK. TROUBLESHOOTING WAS PERFORMED, WHICH INCLUDED REVIEWING ALARM HISTORY, VERIFYING THE USE OF NEW DURACELL BATTERIES, AND CONFIRMING THAT THE BATTERY CAP WAS NOT LOOSE, CRACKED, OR DAMAGED. HOWEVER, THE ISSUE PERSISTED. NO FURTHER PATIENT COMPLICATIONS WERE REPORTED. THE CUSTOMER DISCONTINUED USE OF THE INSULIN PUMP. THE PRODUCT WAS RETURNED FOR ANALYSIS.

  Patient problems: Hyperglycemia

  MAUDE report 22326000 ↗
• MalfunctionJun 25, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED TO MEDTRONIC MINIMED THAT THE CUSTOMER EXPERIENCED HYPERGLYCEMIA. THE BLOOD GLUCOSE VALUE AT THE TIME OF THE EVENT WAS 200 MG/DL. THE CUSTOMER WAS TREATED WITH AN INSULIN PUMP (SUBCUTANEOUS INSULIN INFUSION). THE EVENT INVOLVED PRODUCT(S) MMT-1780KPK. TROUBLESHOOTING WAS NOT PERFORMED. IT WAS UNKNOWN WHETHER THE CUSTOMER WAS USING THE AUTO MODE/SMART GUARD FEATURE AT THE TIME OF THE EVENT. IT WAS UNKNOWN WHETHER THE CUSTOMER WAS USING THE INSULIN PUMP SYSTEM WITHIN 48 HOURS OF THE REPORTED EVENT. NO FURTHER PATIENT COMPLICATIONS WERE REPORTED. THE PRODUCT WAS RETURNED FOR ANALYSIS.

  Patient problems: Hyperglycemia

  MAUDE report 22325847 ↗
• MalfunctionNov 14, 2024Battery Problem; Communication or Transmission Problem; Battery Problem; Communication or Transmission Problem

  IT WAS REPORTED TO MEDTRONIC MINIMED THAT THE CUSTOMER EXPERIENCED LOW BATTERY. THE CUSTOMER REPORTED NO ADVERSE EVENT. THE EVENT INVOLVED PRODUCT(S) MMT-1780KPK. TROUBLESHOOTING WAS PERFORMED. NO HARM REQUIRING MEDICAL INTERVENTION WAS REPORTED. THE CUSTOMER WILL DISCONTINUE THE USE OF THE DEVICE. MMT-1780KPK WAS REQUESTED FOR RETURN AND THE CUSTOMER HAS RETURNED THE DEVICE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 20681710 ↗
• MalfunctionNov 12, 2024Patient Device Interaction Problem; Patient Device Interaction Problem

  IT WAS REPORTED TO MEDTRONIC MINIMED THAT THE CUSTOMER REPORTED PUMP HAD A CRACK THE CUSTOMER REPORTED NO ADVERSE EVENT. THE EVENT INVOLVED PRODUCT(S) MMT-1780KPK. TROUBLESHOOTING WAS PERFORMED. NO HARM REQUIRING MEDICAL INTERVENTION WAS REPORTED. MMT-1780KPKWAS REQUESTED AND CUSTOMER RESPONSE WAS THE DEVICE WILL BE RETURNED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 20661840 ↗
• MalfunctionSep 30, 2024Electrical /Electronic Property Problem; Power Problem; Electrical /Electronic Property Problem; Power Problem

  IT WAS REPORTED TO MEDTRONIC MINIMED THAT THE CUSTOMER REPORTED A PUMP ERROR 23 AND UNEXPECTED BATTERY POWER LOSS. THE CUSTOMER REPORTED NO ADVERSE EVENT. THE EVENT INVOLVED PRODUCT MMT-1780KPK. TROUBLESHOOTING WAS PERFORMED AND ADVISE CUSTOMER TO MONITOR THE PUMP. CUSTOMER MENTIONED LOW BATTERY ALERT LESS THAN 1 WEEK. NO HARM REQUIRING MEDICAL INTERVENTION WAS REPORTED. THE CUSTOMER WILL DISCONTINUE THE USE OF THE DEVICE. MMT-1780KPK WAS RETURNED FOR ANALYSIS.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 20331031 ↗
• MalfunctionSep 26, 2024Power Problem; Power Problem

  IT WAS REPORTED TO MEDTRONIC MINIMED THAT THE CUSTOMER EXPERIENCED UNEXPECTED BATTERY LOSS. THE CUSTOMER REPORTED NO ADVERSE EVENT. TROUBLESHOOTING WAS PERFORMED. THE EVENT INVOLVED PRODUCT(S) MMT-1780KPK. NO HARM REQUIRING MEDICAL INTERVENTION WAS REPORTED. THE CUSTOMER DISCONTINUED THE USE OF THE DEVICE. MMT-1780KPK WAS RETURNED FOR ANALYSIS.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 20308133 ↗
• InjuryJul 4, 2023No Display/Image; No Display/Image

  INFORMATION RECEIVED BY MEDTRONIC INDICATED THAT THE CUSTOMER REPORTED PATIENT WAS ADMITTED IN EMERGENCY ROOM BECAUSE OF HYPERGLYCEMIA AND THE CUSTOMER ALSO REPORTED THAT THE PUMP WAS NOT TURNING ON. THE CUSTOMER¿S BLOOD GLUCOSE LEVEL WAS UNKNOWN. THE CUSTOMER TREATED HIGH BLOOD GLUCOSE WITH EMERGENCY ROOM VISIT. IT WAS UNKNOWN WHETHER THE AUTO MODE FEATURE WAS ACTIVATED AT THE TIME OF HIGH BLOOD GLUCOSE EVENT. CUSTOMER HAD BEEN USING THE INSULIN PUMP SYSTEM WITHIN 48 HOURS OF THE REPORTED HIGH BLOOD GLUCOSE EVENT. TROUBLESHOOTING WAS PERFORMED AND FOUND THAT THE DISPLAY WAS BLANK. NO HARM REQUIRING MEDICAL INTERVENTION WAS REPORTED. THE CUSTOMER WILL DISCONTINUE USING THE INSULIN PUMP AND WILL BE RETURNED FOR ANALYSIS. FRN-UNK-RSVR, UNOMED SET.

  Patient problems: Elevated Ketones/ Diabetic Ketoacidosis; Hyperglycemia

  MAUDE report 17253680 ↗
• MalfunctionJun 19, 2023Device Alarm System; Appropriate Device Problem Term/Code Not Available; Device Alarm System; Appropriate Device Problem Term/Code Not Available

  INFORMATION RECEIVED BY MEDTRONIC INDICATED THAT THE CUSTOMER REPORTED HAD A SENSOR UPDATING ISSUE AND REPORTED THAT THEY DID HEAR THE DIFFERENCES BETWEEN THE TWO AUDIO BEEP VOLUMES. TROUBLESHOOTING WAS PERFORMED. NO HARM REQUIRING MEDICAL INTERVENTION WAS REPORTED. THE CUSTOMER WILL CONTINUE USING THE INSULIN PUMP AND WILL NOT BE RETURNED FOR ANALYSIS

  Patient problems: Hyperglycemia; Hypoglycemia

  MAUDE report 17149668 ↗
• MalfunctionJun 19, 2023Obstruction of Flow; Obstruction of Flow

  INFORMATION RECEIVED BY MEDTRONIC INDICATED THAT THE CUSTOMER REPORTED INSULIN FLOW BLOCK. TROUBLESHOOTING WAS PERFORMED. NO HARM REQUIRING MEDICAL INTERVENTION WAS REPORTED. THE CUSTOMER DISCONTINUED USING THE DEVICE AND THE DEVICE WAS RETURNED FOR ANALYSIS.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 17149660 ↗
• DeathMay 25, 2023Break; Break

  MEDTRONIC LEGAL RECEIVED INFORMATION FROM THE ATTORNEY OF THE FAMILY ON APRIL 18, 2023. THE REPORTER ALLEGES THAT THE USE OF ONE OR MORE MEDTRONIC MINI MED 600 SERIES INSULIN PUMPS WITH A DAMAGED, MISSING, OR BROKEN RETAINER RING CAUSED THE CLAIMANT TO SUFFER PERSONAL INJURIES . THE ALLEGATION DID NOT SPECIFY THE PUMP IDENTIFIER (SERIAL NUMBER) AND THEREFORE ALL 600 SERIES INSULIN PUMPS IN POSSESSION OF THE CLAIMANT, INCLUDING THIS PUMP, ARE CONSIDERED POTENTIALLY WITHIN THE SCOPE OF THE REPORT PENDING CONFIRMATION OF THE AFFECTED SERIAL NUMBER(S). ALL RELATED REPORTS WILL BE UPDATED ACCORDINGLY WHEN AND IF THE AFFECTED SERIAL NUMBER WAS IDENTIFIED. THE CUSTOMER WAS PASSED AWAY AT HOME ON (B)(6) 2020. THE CAUSE OF DEATH WAS MENTAL ILLNESS. THE CUSTOMER¿S BLOOD GLUCOSE WAS UNKNOWN. THE CUSTOMER WAS WEARING THE INSULIN PUMP AT THE TIME OF DEATH. NO FURTHER PATIENT COMPLICATIONS WERE REPORTED. THE INSULIN PUMP WILL BE RETURNED FOR ANALYSIS.

  Patient problems: Insufficient Information

  MAUDE report 17000267 ↗
• MalfunctionMay 5, 2023Obstruction of Flow; Obstruction of Flow

  INFORMATION RECEIVED BY MEDTRONIC INDICATED THAT THE INSULIN PUMP OCCLUDED DURING THERAPY. BLOOD GLUCOSE VALUE AT THE TIME OF EVENT WAS 243 MG/DL. NO HARM REQUIRING MEDICAL INTERVENTION WAS REPORTED. TROUBLESHOOTING WAS PERFORMED AND CUSTOMER WAS ABLE TO RESOLVE THE ISSUE. THE PRODUCT WILL BE RETURNED FOR ANALYSIS.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 16874103 ↗
• MalfunctionFeb 16, 2023Circuit Failure; Communication or Transmission Problem; Circuit Failure; Communication or Transmission Problem

  INFORMATION RECEIVED BY MEDTRONIC INDICATED THAT THE CUSTOMER RECEIVED A PUMP ERROR 4 AND 63 ALARM. NO HARM REQUIRING MEDICAL INTERVENTION WAS REPORTED. TROUBLESHOOTING WAS PERFORMED AND THE CUSTOMER WAS ABLE TO CLEAR THE ALARM SUCCESSFULLY AND STATED THAT THE PUMP REWIND WAS COMPLETED. THE CUSTOMER WILL DISCONTINUE USING THE INSULIN PUMP AND WILL BE RETURNED FOR ANALYSIS.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 16384369 ↗
• MalfunctionFeb 15, 2023Circuit Failure; Electrical /Electronic Property Problem; Circuit Failure; Electrical /Electronic Property Problem

  INFORMATION RECEIVED BY MEDTRONIC INDICATED THAT THE INSULIN PUMP HA MULTIPLE INSULIN PUMP ERROR ALARMS. CUSTOMER WAS UNABLE TO CLEAR THE ALARM. CUSTOMER WAS UNABLE TO REWIND THE INSULIN PUMP. NO HARM REQUIRING MEDICAL INTERVENTION WAS REPORTED. THE INSULIN PUMP WAS RETURNED FOR ANALYSIS.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 16377835 ↗
• MalfunctionJan 30, 2023Circuit Failure; Circuit Failure

  INFORMATION RECEIVED BY MEDTRONIC INDICATED THAT THE INSULIN PUMP HAD A HARDWARE LOW LEVEL FAILURE ALARM. CUSTOMER WAS ABLE TO CLEARED ALARM AND WAS ABLE TO COMPLETE REWIND. CUSTOMER STATED THAT THE ALARM OCCURRED SECOND TIME AND THIRD TIME IT WAS SHUT DOWN ON, EVEN WITH NEW BATTERIES AND IT WAS NOT ALLOWING BACK INTO AUTO MODE SAYING ACTIVE INSULIN UPDATING. TROUBLESHOOTING WAS PERFORMED. NO HARM REQUIRING MEDICAL INTERVENTION WAS REPORTED. THE DEVICE WAS RETURNED FOR ANALYSIS.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 16264766 ↗
• InjuryJan 6, 2023Break; Break

  THE CUSTOMER REPORTED VIA PHONE CALL THAT THEY WERE HOSPITALIZED DUE TO LOW BLOOD GLUCOSE UNKNOWN DATE WITH BLOOD GLUCOSE LEVEL WAS 20 MG/DL. THE CURRENT VALUE OF BLOOD GLUCOSE LEVEL WAS 225MG/DL. CUSTOMER REPORTED CRACK AT BACK SIDE. CUSTOMER FELL ON INSULIN PUMP AND PASSED OUT. TROUBLESHOOTING WAS PERFORMED. THE INSULIN PUMP WAS RETURNED FOR ANALYSIS.

  Patient problems: Hypoglycemia; Loss of consciousness

  MAUDE report 16110477 ↗
• MalfunctionSep 13, 2022Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT THE CUSTOMER HAD PASSED AWAY ON (B)(6) 2020 AT HOSPITAL. THE CUSTOMER WAS HOSPITALIZED ON AN UNKNOWN DATE DUE TO UNKNOWN REASON. THE CAUSE OF DEATH WAS UNKNOWN. THE CUSTOMER BLOOD GLUCOSE WAS 230 MG/DL AT THE TIME OF DEATH. IT WAS UNKNOWN WHETHER THE AUTO MODE WAS ACTIVE OR NOT AT THE TIME OF DEATH. THE INSULIN PUMP WAS RETURNED FOR THE ANALYSIS. THE CASE WAS REPORTED ON THE BASIS OF FAILURE ANALYSIS.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 15408037 ↗
• MalfunctionAug 29, 2022Patient Device Interaction Problem; Patient Device Interaction Problem

  INFORMATION RECEIVED BY MEDTRONIC INDICATED THAT THE INSULIN PUMP HAD MISSING RETAINER RING. RESERVOIR WAS ABLE TO LOCKED IN PLACE. NO HARM REQUIRING MEDICAL INTERVENTION WAS REPORTED. TROUBLESHOOTING WAS PERFORMED; HOWEVER, THE CUSTOMER WILL DISCONTINUE USE OF THE DEVICE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 15310589 ↗
• MalfunctionAug 5, 2022Break; Break

  MEDTRONIC RECEIVED INFORMATION THAT DAMAGE (PHYSICAL OR COSMETIC) OCCURRED. THERE WAS NO ADVERSE IMPACT OR CONSEQUENCE REPORTED AS A RESULT OF THIS EVENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 15172437 ↗
• MalfunctionAug 4, 2022Break; Break

  INFORMATION RECEIVED FROM MEDTRONIC INDICATED THAT THE INSULIN PUMP HAD DAMAGED RETAINER RING. NO HARM REQUIRING MEDICAL INTERVENTION WAS REPORTED. THE INSULIN PUMP WAS RETURNED FOR ANALYSIS.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 15162576 ↗
• MalfunctionAug 4, 2022Break; No Apparent Adverse Event; Break; No Apparent Adverse Event

  INFORMATION RECEIVED BY MEDTRONIC INDICATED THAT THE INSULIN PUMP RETAINER RING WAS CHIPPED OFF. THE CUSTOMER STATED THAT THE RESERVOIR WAS ABLE TO LOCK IN PLACE. NO HARM REQUIRING MEDICAL INTERVENTION WAS REPORTED. THE DEVICE WAS RETURNED FOR ANALYSIS.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 15162259 ↗
• MalfunctionAug 2, 2022Break; Break

  MEDTRONIC RECEIVED INFORMATION THAT DAMAGE (PHYSICAL OR COSMETIC) OCCURRED. THERE WAS NO ADVERSE IMPACT OR CONSEQUENCE REPORTED AS A RESULT OF THIS EVENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 15149912 ↗
• MalfunctionAug 2, 2022Break; Break

  INFORMATION RECEIVED BY MEDTRONIC INDICATED THAT THE INSULIN PUMP HAD CRACKED RETAINER RING. THE RESERVOIR IS ABLE TO LOCK IN PLACE. CUSTOMER REPORTED CHANGE SENSOR AND CALIBRATION NOT ACCEPTED. NO HARM REQUIRING MEDICAL INTERVENTION WAS REPORTED. THE DEVICE WILL BE RETURNED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 15146794 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under P160017. One submission often covers many models, so check the product and lot details in each record.

• Z-2981-2026 · Jul 13, 2026 · Open, Classified
  MiniMed 670G Insulin Pump, Model: MMT-1781, MMT-1782;
• Z-1742-2026 · Feb 13, 2026 · Open, Classified
  MiniMed 770G Insulin Pump (MMT-1880, MMT-1881, MMT-1882, MMT-1890, MMT-1891, MMT-1892)
• Z-1266-2025 · Jan 31, 2025 · Open, Classified
  MiniMed insulin pump, REF: 780G (MMT-1884, MMT-1885, MMT-1886, MMT-1894, MMT-1895, MMT-1896)
• Z-1265-2025 · Jan 31, 2025 · Open, Classified
  MiniMed insulin pump, REF: 770G (MMT-1880, MMT-1881, MMT-1882, MMT-1890, MMT-1891, MMT-1892)
• Z-1261-2025 · Jan 31, 2025 · Open, Classified
  MiniMed insulin pump, REF: 670G (MMT-1760, MMT-1761, MMT-1762, MMT-1780, MMT-1781, MMT-1782)
• Z-0193-2023 · Sep 20, 2022 · Open, Classified
  Insulin Pump/Model: MiniMed 630G/ MMT-1715, MMT-1755, MMT-1754; MiniMed 670G/ MMT-1780, MMT-1781, MMT-1782, MMT-1760, MMT-1761, MMT-1762, MMT-1740, MMT-1741, MMT-1742
• Z-0855-2022 · Jan 27, 2022 · Open, Classified
  MiniMed 630G: MMT-1715, MMT-1754, MMT-1755; MiniMed 670G: MMT-1740, MMT-1741, MMT-1742, MMT-1760, MMT-1761, MMT-1762, MMT-1780, MMT-1781, MMT-1782; MiniMed 770G: MMT-1880, MMT-1881
• Z-1771-2021 · Mar 15, 2021 · Open, Classified
  MiniMed 780G Insulin Pump: Models: PUMP MMT-1885 MM780G 6.5V BLE MMOL; PUMP MMT-1886 MM780G 6.5W BLE MG; KIT MMT-1895WW MM780G 6.5V BLE SF MMOL; KIT MMT-1896WW MM780G 6.5W BLE SF M
• Z-0516-2021 · Apr 30, 2020 · Open, Classified
  MiniMed 670G, insulin pump, Ref/Model # MMT-1760KPK, MMT-1762KCN, MMT-1762WWK - Product Usage: indicated for continuous or periodic monitoring of glucose levels in the fluid under
• Z-0956-2020 · Nov 21, 2019 · Open, Classified
  Medtronic MiniMed 670G System with SmartGuard, Ref #s/Model Number(s) - MMT-1741, MMT-1742, MMT-1760, MMT-1761, MMT-1762, MMT-1580, MMT-1581, MMT-1582, MMT-1780, MMT-1781, and MM
• Z-2605-2017 · May 8, 2017 · Terminated
  MiniMed 670G Insulin Infusion Pump, Catalog No. MMT-1580, MMT-1780, MMT-1782, MMT-1760.
• Z-2604-2017 · May 8, 2017 · Terminated
  MiniMed 640G Insulin Infusion Pump, Catalog No. MMT-1511, MMT-1711, MMT-1512, MMT-1712, MMT-1551, MMT-1751, MMT-1552, MMT-1752.