MiniMed® 670G MMT-1780KPK (UDI 00643169939219)Recalls & reported problems

Summary

The FDA's MAUDE database contains 55,723 adverse event reports that list this exact device (DI 00643169939219), received between Jun 2, 2017 and Sep 19, 2025 — classified as 78 deaths, 12,937 injuries, 42,708 malfunctions.

The most frequently reported specific device problem is “Patient Device Interaction Problem” (18,235 reports).

3 FDA recall records name this device's identifier, 3 still open.

11 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 ↗

3. Sep 20, 2022Class IIOpen, Classified

   Medtronic identified a cybersecurity vulnerability in the MiniMed 600 series Insulin Pump Systems associated with the communication protocol that could allow unauthorized access to the pump system. This unauthorized access could be used to deliver too much or too little insulin through delivery of an unintended insulin bolus or because insulin delivery is slowed or stopped, which could lead to hypoglycemia or hyperglycemia. The Remote Bolus feature on insulin pumps should be turned off to prevent the unauthorized access.

   Z-0193-2023 · Root cause: Component change control · Recall details · FDA record ↗

Most reported problems

Recent adverse event reports

The 25 most recent of 55,723 reports, in the reporter's own words as published by the FDA.

• MalfunctionSep 19, 2025Material Integrity Problem; Material Integrity Problem

  IT WAS REPORTED TO MEDTRONIC MINIMED THAT THE CUSTOMER EXPERIENCED COSMETIC DAMAGE. THE CUSTOMER REPORTED NO ADVERSE EVENT. THE EVENT INVOLVED PRODUCT(S) MMT-1780KPK. TROUBLESHOOTING WAS NOT PERFORMED. NO HARM REQUIRING MEDICAL INTERVENTION WAS REPORTED. THE CUSTOMER WILL DISCONTINUE THE USE OF THE PUMP AND REVERT TO A BACKUP PLAN PER HEALTHCARE PROFESSIONAL INSTRUCTIONS. MMT-1780KPK WAS REQUESTED AND CUSTOMER RESPONSE WAS THE DEVICE RETURNED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 23095113 ↗
• 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 HIGH BLOOD GLUCOSE READINGS WHILE FLYING AND WEARING A MASK, AS WELL AS NEEDING ASSISTANCE WITH UPLOADING THEIR PUMP TO CARELINK. THE CUSTOMER REPORTED NO ADVERSE EVENT. THE EVENT INVOLVED PRODUCT(S) MMT-1780KPK AND ACC-7350. TROUBLESHOOTING WAS DECLINED BY THE CUSTOMER. NO HARM REQUIRING MEDICAL INTERVENTION WAS REPORTED. NO PRODUCT RETURN IS REQUIRED FOR MMT-1780KPK. NO PRODUCT RETURN IS REQUIRED FOR ACC-7350.

  Patient problems: Hyperglycemia

  MAUDE report 22409686 ↗
• MalfunctionJul 7, 2025Excess Flow or Over-Infusion; Excess Flow or Over-Infusion

  IT WAS REPORTED TO MEDTRONIC MINIMED THAT THE CUSTOMER EXPERIENCED OVER-DELIVERY OF INSULIN DURING AIR TRAVEL. THE CUSTOMER REPORTED SEVERE HYPOGLYCEMIA DURING FLIGHTS AND SEVERE HYPERGLYCEMIA POST-FLIGHT. THE EVENT INVOLVED PRODUCT(S) MMT-1780KPK. TROUBLESHOOTING WAS NOT PERFORMED. NO HARM REQUIRING MEDICAL INTERVENTION WAS REPORTED. NO PRODUCT RETURN IS REQUIRED FOR MMT-1780KPK.

  Patient problems: Hyperglycemia; Hypoglycemia

  MAUDE report 22409560 ↗
• MalfunctionJul 7, 2025Wireless Communication Problem; Wireless Communication Problem

  IT WAS REPORTED TO MEDTRONIC MINIMED THAT THE CUSTOMER EXPERIENCED A LOW BLOOD GLUCOSE LEVEL AND HEAD PAIN DURING A FLIGHT DESCENT. THE CUSTOMER INQUIRED ABOUT USING AIRPLANE MODE ON THE PUMP DURING FLIGHTS. THE EVENT INVOLVED PRODUCT(S) MMT-1780KPK. TROUBLESHOOTING WAS PERFORMED, AND THE CUSTOMER REPORTED THAT THE PUMP AND GLUCOMETER WERE NOT CONNECTING. NO HARM REQUIRING MEDICAL INTERVENTION WAS REPORTED. THE PRODUCT WAS NOT RETURNED FOR ANALYSIS.

  Patient problems: Hypoglycemia; Pain

  MAUDE report 22409530 ↗
• 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 HYPOGLYCEMIA. THE CUSTOMER ALSO REPORTED THAT THE HYPOGLYCEMIA EVENT OCCURRED DURING THE FLIGHT JOURNEY. BLOOD GLUCOSE VALUE AT THE TIME OF EVENT WAS 70 MG/DL. THE CUSTOMER WAS TREATED WITH CARBOHYDRATE INTAKE. THE EVENT INVOLVED PRODUCT(S) MMT-1780KPK. TROUBLESHOOTING WAS NOT PERFORMED. NO FURTHER PATIENT COMPLICATIONS WERE REPORTED. NO PRODUCT RETURN IS REQUIRED FOR MMT-1780KPK.

  Patient problems: Hypoglycemia

  MAUDE report 22409508 ↗
• MalfunctionJul 3, 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 HYPOGLYCEMIA AFTER A FLIGHT AND HAD ISSUES CALIBRATING THE SENSOR. THE CUSTOMER ALSO REPORTED THAT THE INSULIN PUMP WAS NOT PUT INTO FLIGHT MODE DURING THE FLIGHT. BLOOD GLUCOSE VALUE AT THE TIME OF THE EVENT WAS 61 MG/DL. THE CUSTOMER WAS TREATED WITH GLUCOSE TABLETS. THE EVENT INVOLVED PRODUCT(S) MMT-1780KPK. TROUBLESHOOTING WAS PERFORMED, INCLUDING ASSISTING THE CUSTOMER WITH DELETING AND RELINKING THE TRANSMITTER AND ADVISING ON THE USE OF THE CHARGER FOR RE-PAIRING. THE CUSTOMER WAS ADVISED TO MONITOR SENSOR USAGE AND REMEMBER TO REMOVE IT ON TIME. NO FURTHER PATIENT COMPLICATIONS WERE REPORTED. NO PRODUCT RETURN IS REQUIRED FOR MMT-1780KPK.

  Patient problems: Hypoglycemia

  MAUDE report 22394345 ↗
• MalfunctionJul 3, 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 THE BLOOD GLUCOSE INCREASED AFTER GETTING OFF THE PLANE. BLOOD GLUCOSE VALUE AT THE TIME OF EVENT WAS 344 MG/DL. THE CUSTOMER WAS TREATED WITH INSULIN PUMP (SUBCUTANEOUS INSULIN INFUSION). THE EVENT INVOLVED PRODUCT(S) MMT-1780KPK. TROUBLESHOOTING WAS PERFORMED. NO FURTHER PATIENT COMPLICATIONS WERE REPORTED. NO PRODUCT RETURN IS REQUIRED FOR MMT-1780KPK.

  Patient problems: Hyperglycemia

  MAUDE report 22394334 ↗
• MalfunctionJul 3, 2025Break; Battery Problem; Break; Battery Problem

  IT WAS REPORTED TO MEDTRONIC MINIMED THAT THE CUSTOMER RECEIVED A SHORT BATTERY LIFE, REPLACE BATTERY NOW ALARMS, AND PHYSICAL DAMAGE TO THEIR INSULIN PUMP. THE CUSTOMER REPORTED NO ADVERSE EVENT. THE EVENT INVOLVED PRODUCT(S) MMT-1780KPK. TROUBLESHOOTING WAS PERFORMED AND THE CUSTOMER REPORTED A CRACK ALONG THE BATTERY CYLINDER. AFTER REPLACING THE BATTERY MULTIPLE TIMES, THE PUMP CONTINUED TO EXPERIENCE ALARMS, AND THE BATTERY LIFE DID NOT EXCEED ONE DAY. NO HARM REQUIRING MEDICAL INTERVENTION WAS REPORTED. THE PRODUCT WAS RETURNED FOR ANALYSIS.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22392989 ↗
• MalfunctionJul 3, 2025Wireless Communication Problem; Wireless Communication Problem

  IT WAS REPORTED TO MEDTRONIC MINIMED THAT THE CUSTOMER EXPERIENCED ISSUES WITH THEIR INSULIN PUMP AND TRANSMITTER, AND DIFFICULTY ENTERING AUTO MODE AND RECURRING SENSOR AND TRANSMITTER PROBLEMS. THE CUSTOMER REPORTED NO ADVERSE EVENT. THE EVENT INVOLVED PRODUCT(S) MMT-7020A. TROUBLESHOOTING WAS PERFORMED, BUT THE ISSUE WAS NOT RESOLVED. NO HARM REQUIRING MEDICAL INTERVENTION WAS REPORTED. THE PRODUCT WAS RETURNED FOR ANALYSIS.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22392489 ↗
• MalfunctionJun 25, 2025Battery Problem; Battery Problem

  IT WAS REPORTED TO MEDTRONIC MINIMED THAT THE CUSTOMER EXPERIENCED RAPID BATTERY DEPLETION, WITH THE PUMP REQUIRING A BATTERY CHANGE EVERY 24 HOURS DESPITE USING BOTH ALKALINE AND LITHIUM BATTERIES. THE CUSTOMER REPORTED NO ADVERSE EVENT. THE EVENT INVOLVED PRODUCT(S) MMT-1780KPK. TROUBLESHOOTING WAS PERFORMED THAT INCLUDED REVIEWING ALARM HISTORY, ADJUSTING SETTINGS SUCH AS BACKLIGHT TIMEOUT AND VIBRATION MODE, AND PERFORMING A PUMP RESTART, BUT THE ISSUE PERSISTED. NO HARM REQUIRING MEDICAL INTERVENTION WAS REPORTED. THE PRODUCT WAS RETURNED FOR ANALYSIS.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22326070 ↗
• MalfunctionJun 25, 2025Battery Problem; Battery Problem

  IT WAS REPORTED TO MEDTRONIC MINIMED THAT THE CUSTOMER EXPERIENCED FREQUENT "REPLACE BATTERY" AND "REPLACE BATTERY NOW" ALERTS, WITH THE ISSUE PERSISTING DESPITE REPLACING THE BATTERY CAP AND USING NEW ENERGIZER BATTERIES. THE CUSTOMER REPORTED NO ADVERSE EVENT. THE EVENT INVOLVED PRODUCT(S) MMT-1780KPK. TROUBLESHOOTING WAS PERFORMED THAT INCLUDED REVIEWING ALARM HISTORY AND VERIFYING BATTERY USAGE, BUT THE ISSUE PERSISTED. NO HARM REQUIRING MEDICAL INTERVENTION WAS REPORTED. THE PRODUCT WAS RETURNED FOR ANALYSIS.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22325840 ↗
• MalfunctionJun 25, 2025Battery Problem; Battery Problem

  IT WAS REPORTED TO MEDTRONIC MINIMED THAT THE CUSTOMER EXPERIENCED RAPID BATTERY DEPLETION, WITH THE BATTERY LASTING ONLY FOUR DAYS AND RECEIVING MULTIPLE "LOW BATTERY" AND "REPLACE BATTERY NOW" ALERTS LESS THAN 8 HOURS APART. THE CUSTOMER REPORTED NO ADVERSE EVENT. THE EVENT INVOLVED PRODUCT(S) MMT-1780KPK. TROUBLESHOOTING WAS PERFORMED THAT INCLUDED REVIEWING ALARM HISTORY AND VERIFYING BATTERY USAGE AND CONDITION, BUT THE ISSUE PERSISTED. NO HARM REQUIRING MEDICAL INTERVENTION WAS REPORTED. THE PRODUCT WAS RETURNED FOR ANALYSIS.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22325831 ↗
• MalfunctionJun 25, 2025Battery Problem; Battery Problem

  IT WAS REPORTED TO MEDTRONIC MINIMED THAT THE CUSTOMER EXPERIENCED SHORT BATTERY LIFE, WITH THE PUMP REQUIRING A BATTERY CHANGE EVERY TWO DAYS AND RECEIVING A "REPLACE BATTERY NOW" ALARM. THE CUSTOMER REPORTED NO ADVERSE EVENT. THE EVENT INVOLVED PRODUCT(S) MMT-1780KPK. TROUBLESHOOTING WAS PERFORMED, INCLUDING REVIEWING ALARM HISTORY, BUT THE ISSUE PERSISTED. NO HARM REQUIRING MEDICAL INTERVENTION WAS REPORTED. THE PRODUCT WAS RETURNED FOR ANALYSIS.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22325713 ↗
• MalfunctionJun 25, 2025Battery Problem; Battery Problem

  IT WAS REPORTED TO MEDTRONIC MINIMED THAT THE CUSTOMER EXPERIENCED SHORT BATTERY LIFE, WITH THE BATTERY LASTING LESS THAN ONE WEEK DESPITE USING ENERGIZER LITHIUM BATTERIES. THE CUSTOMER REPORTED NO ADVERSE EVENT. THE EVENT INVOLVED PRODUCT(S) MMT-1780KPK. TROUBLESHOOTING WAS PERFORMED THAT INCLUDED REVIEWING ALARM HISTORY, INSPECTING THE BATTERY CAP AND COMPARTMENT FOR DAMAGE OR CORROSION, AND ADJUSTING PUMP SETTINGS, BUT THE ISSUE PERSISTED. NO HARM REQUIRING MEDICAL INTERVENTION WAS REPORTED. THE PRODUCT WAS RETURNED FOR ANALYSIS.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22325703 ↗
• MalfunctionJun 25, 2025Battery Problem; Battery Problem

  IT WAS REPORTED TO MEDTRONIC MINIMED THAT THE CUSTOMER EXPERIENCED RAPID BATTERY DEPLETION, WITH BATTERIES LASTING ONLY 3 TO 4 DAYS, AND MULTIPLE LOW BATTERY AND REPLACE BATTERY NOW ALERTS. THE CUSTOMER REPORTED NO ADVERSE EVENT. THE EVENT INVOLVED PRODUCT(S) MMT-1780KPK. TROUBLESHOOTING WAS PERFORMED, INCLUDING REVIEWING ALARM HISTORY, ADJUSTING SETTINGS SUCH AS BACKLIGHT TIMEOUT AND AUDIO MODE, AND PERFORMING A PUMP RESTART. THE CUSTOMER WAS ADVISED TO USE AA LITHIUM BATTERIES FOR BEST RESULTS, MONITOR THE PUMP, AND CALL BACK IF THE ISSUE PERSISTED. NO HARM REQUIRING MEDICAL INTERVENTION WAS REPORTED. THE PRODUCT WAS RETURNED FOR ANALYSIS.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22325582 ↗
• MalfunctionJun 25, 2025Battery Problem; Battery Problem

  IT WAS REPORTED TO MEDTRONIC MINIMED THAT THE CUSTOMER EXPERIENCED LOW BATTERY LIFE, WITH THE BATTERY LASTING ONLY 2-3 DAYS, DESPITE USING DIFFERENT TYPES OF BATTERIES, INCLUDING LITHIUM. THE CUSTOMER REPORTED NO ADVERSE EVENT. THE EVENT INVOLVED PRODUCT(S) MMT-1780KPK. TROUBLESHOOTING WAS NOT PERFORMED DUE TO THE CUSTOMER PREVIOUSLY REPORTING THE SAME ISSUE MULTIPLE TIMES. NO HARM REQUIRING MEDICAL INTERVENTION WAS REPORTED. THE PRODUCT WAS REPLACED AND RETURNED FOR ANALYSIS.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22325498 ↗
• MalfunctionJun 25, 2025Battery Problem; Battery Problem

  IT WAS REPORTED TO MEDTRONIC MINIMED THAT THE CUSTOMER EXPERIENCED LOW BATTERY LIFE, WITH THE BATTERY LASTING LESS THAN ONE WEEK, AND FREQUENT REPLACE BATTERY NOW ALARMS WITH THE INSULIN PUMP. THE CUSTOMER REPORTED NO ADVERSE EVENT. THE EVENT INVOLVED PRODUCT(S) MMT-1780KPK. TROUBLESHOOTING WAS PERFORMED, BUT THE ISSUE PERSISTED. NO HARM REQUIRING MEDICAL INTERVENTION WAS REPORTED. THE PRODUCT WAS REPLACED AND RETURNED FOR ANALYSIS.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22325490 ↗
• MalfunctionJun 25, 2025Battery Problem; Battery Problem

  IT WAS REPORTED TO MEDTRONIC MINIMED THAT THE CUSTOMER EXPERIENCED RAPID BATTERY DEPLETION, WITH THE PUMP REQUIRING A NEW BATTERY FIVE TIMES IN THE LAST FIVE DAYS DESPITE USING ENERGIZER LITHIUM BATTERIES. THE CUSTOMER REPORTED NO ADVERSE EVENT. THE EVENT INVOLVED PRODUCT(S) MMT-1780KPK. TROUBLESHOOTING WAS PERFORMED, INCLUDING VERIFYING BATTERY USAGE, PUMP SETTINGS, AND ALARM HISTORY, AND PROVIDING SUGGESTIONS TO OPTIMIZE BATTERY LIFE. HOWEVER, THE ISSUE PERSISTED. NO HARM REQUIRING MEDICAL INTERVENTION WAS REPORTED. THE PRODUCT WAS RETURNED FOR ANALYSIS.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22325482 ↗
• MalfunctionJun 25, 2025Battery Problem; Battery Problem

  IT WAS REPORTED TO MEDTRONIC MINIMED THAT THE CUSTOMER EXPERIENCED LOW BATTERY ISSUES, AND THE BATTERY LASTING ONLY A FEW DAYS EVEN AFTER REPLACING THE BATTERY. THE CUSTOMER REPORTED NO ADVERSE EVENT. THE EVENT INVOLVED PRODUCT MMT-1780KPK. TROUBLESHOOTING WAS NOT PERFORMED DURING THIS CALL. NO HARM REQUIRING MEDICAL INTERVENTION WAS REPORTED. THE PRODUCT WAS RETURNED FOR ANALYSIS.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22325372 ↗
• MalfunctionSep 26, 2024No Display/Image; Patient Device Interaction Problem; No Display/Image; Patient Device Interaction Problem

  IT WAS REPORTED TO MEDTRONIC MINIMED THAT THE CUSTOMER EXPERIENCED PUMP WON¿T TURN BACK ON AND UNABLE TO READ. THE CUSTOMER REPORTED NO ADVERSE EVENT. THE EVENT INVOLVED PRODUCT MMT-1780KPK. TROUBLESHOOTING WAS PERFORMED AND CUSTOMER WAS ADVISED THAT PUMP IS STILL USABLE BUT TO MONITOR IT. 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 20308215 ↗
• MalfunctionSep 26, 2024Battery Problem; Battery Problem

  IT WAS REPORTED TO MEDTRONIC MINIMED THAT THE CUSTOMER EXPERIENCED LOW/SHORT BATTERY LIFETIME. 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 DISCONTINUED TO USE THE DEVICE, MMT-1780KPK WAS REQUESTED AND THE CUSTOMER RESPONSE WAS THE DEVICE RETURNED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 20308142 ↗
• MalfunctionSep 26, 2024Power Problem; Power Problem

  IT WAS REPORTED TO MEDTRONIC MINIMED THAT THE CUSTOMER REPLACED A BRAND NEW BATTERY MULTIPLE TIMES AND THE PUMP DIED DOWN AFTER A FEW HOURS. THE CUSTOMER REPORTED NO ADVERSE EVENT. THE EVENT INVOLVED PRODUCT(S) MMT-1780KPK. TROUBLESHOOTING WAS PERFORMED FOR SHORT BATTERY LIFETIME. NO HARM REQUIRING MEDICAL INTERVENTION WAS REPORTED. THE CUSTOMER WILL DISCONTINUE THE USE OF THE DEVICE. THE MMT-1780KPK WAS RETURNED FOR PRODUCT ANALYSIS.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 20307857 ↗
• MalfunctionSep 22, 2024Circuit Failure; Loss of Data; Environmental Compatibility Problem; Patient Device Interaction Problem; Circuit Failure; Loss of Data; Environmental Compatibility Problem; Patient Device Interaction Problem

  IT WAS REPORTED TO MEDTRONIC MINIMED THAT THE CUSTOMER EXPERIENCED HYPERGLYCEMIA. THE CUSTOMER REPORTED BLOOD GLUCOSE VALUE OF 342 MG/DL. THE CUSTOMER EXPERIENCED PUMP STICKER WORN OUT AND UNABLE TO SEE THE SERIAL NUMBER ON THE BACK. AND THE CUSTOMER RECEIVED PUMP ERROR 63, 45 AND 22. THE EVENT INVOLVED PRODUCT(S) MMT-1780KPK. TROUBLESHOOTING WAS PERFORMED FOR COSMETIC DAMAGE AND PUMP ERROR ALARMS. ADVISED CUSTOMER TO REPLACE THE PUMP. NO HARM REQUIRING MEDICAL INTERVENTION WAS REPORTED. THE CUSTOMER WILL DISCONTINUE THE USE OF THE DEVICE. THE MMT-1780KPK WAS RETURNED FOR PRODUCT ANALYSIS.

  Patient problems: Hyperglycemia

  MAUDE report 20276070 ↗
• MalfunctionSep 13, 2024Break; Break

  IT WAS REPORTED TO MEDTRONIC MINIMED THAT THE CUSTOMER EXPERIENCED DAMAGE (PHYSICAL OR COSMETIC). THE CUSTOMER REPORTED NO ADVERSE EVENT. THE EVENT INVOLVED PRODUCT(S) MMT-1780KPK. TROUBLESHOOTING WAS PERFORMED. CUSTOMER REPORTED THAT PUMP WAS DROPPED AND THE DAMAGE WAS NOT RELATED TO THE RETAINER RING. NO HARM REQUIRING MEDICAL INTERVENTION WAS REPORTED. THE CUSTOMER WILL DISCONTINUE THE USE OF THE DEVICE. MMT-1780KPK WAS REQUESTED FOR RETURN AND CUSTOMER HAS RETURNED THE DEVICE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 20209210 ↗
• MalfunctionAug 9, 2024Break; Appropriate Device Problem Term/Code Not Available; Break; Appropriate Device Problem Term/Code Not Available

  MEDTRONIC LEGAL RECEIVED INFORMATION FROM THE ATTORNEY OF THE FAMILY ON (B)(6) 2018. THE REPORTER ALLEGED 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, WERE CONSIDERED POTENTIALLY WITHIN THE SCOPE OF THE REPORT PENDING CONFIRMATION OF THE AFFECTED SERIAL NUMBER(S). WHEN AND IF THE AFFECTED SERIAL NUMBER WAS IDENTIFIED, ALL RELATED REPORTS WILL BE UPDATED ACCORDINGLY. NO PRODUCT RETURN IS REQUIRED FOR THE PRODUCT.

  Patient problems: Insufficient Information

  MAUDE report 19947137 ↗

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-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.