Guardian™ Sensor (3) MMT-7020A (UDI 20763000140940)Recalls & reported problems

Summary

The FDA's MAUDE database contains 1,304 adverse event reports that list this exact device (DI 20763000140940), received between Aug 30, 2018 and Jun 30, 2022 — classified as 121 injuries, 1,183 malfunctions.

The most frequently reported specific device problem is “Incorrect, Inadequate or Imprecise Result or Readings” (975 reports).

14 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.

Most reported problems

Recent adverse event reports

The 25 most recent of 1,304 reports, in the reporter's own words as published by the FDA.

• MalfunctionJun 30, 2022Calibration Problem; Calibration Problem

  MEDTRONIC RECEIVED INFORMATION THAT BATTERY CAP CRACKED/DAMAGED 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 14876841 ↗
• MalfunctionJul 20, 2021Break; Break

  INFORMATION RECEIVED BY MEDTRONIC INDICATED THAT THE INTRODUCES NEEDLE FRACTURED WHILE IN THE BODY. CUSTOMER MENTIONED THAT SENSOR FELL OFF RIGHT AFTER INSERTION. CUSTOMER STATED THAT THE ISSUE WAS OCCURRED PRIOR TO INSERTION. CUSTOMER STATED THAT THE NEEDLE WAS DETACHED. CUSTOMER REPORTED THE SENSOR WAS NO LONGER IN THE BODY. CUSTOMER REPORTED THAT THEY DID NOT RECEIVE MEDICAL TREATMENT AS A RESULT OF THE SENSOR FRACTURING WHILE STILL IN THE BODY. THE SENSOR WILL NOT BE RETURNED FOR ANALYSIS.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 12194896 ↗
• MalfunctionAug 13, 2020Incorrect, Inadequate or Imprecise Result or Readings; Unexpected Therapeutic Results; Incorrect, Inadequate or Imprecise Result or Readings; Unexpected Therapeutic Results

  INFORMATION RECEIVED BY MEDTRONIC THE USER REPORTED INACCURATE SENSOR READINGS THAT TRIGGERED A THRESHOLD SUSPEND. THE CUSTOMER¿S BLOOD GLUCOSE WAS 188 MG/DL AND SENSOR GLUCOSE WAS 86 MG/DL AT THE TIME OF THE EVENT, THE DIFFERENCE IS OUTSIDE THE ACCEPTABLE RANGE. NO HARM REQUIRING MEDICAL INTERVENTION WAS REPORTED. THE SENSOR WILL NOT BE RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 10400302 ↗
• MalfunctionAug 10, 2020Incorrect, Inadequate or Imprecise Result or Readings; Calibration Problem; Incorrect, Inadequate or Imprecise Result or Readings; Calibration Problem

  INFORMATION RECEIVED BY MEDTRONIC INDICATED THAT THE SENSOR HAD INACCURATE READINGS THAT TRIGGERED THRESHOLD SUSPEND ALARM. THE CUSTOMER¿S BLOOD GLUCOSE WAS 91MG/DL AND THE SENSOR GLUCOSE WAS 40 MG/DL. INSULIN DELIVERY WAS SUSPEND DUE TO SENSOR VALUES. CUSTOMER STATED INSULIN PUMP RECEIVED CALIBRATION NOT ACCEPTED AND CHANGE SENOR ALERT. THE SENSOR WILL NOT BE RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 10384244 ↗
• MalfunctionAug 7, 2020Incorrect, Inadequate or Imprecise Result or Readings; Calibration Problem; Incorrect, Inadequate or Imprecise Result or Readings; Calibration Problem

  INFORMATION RECEIVED BY MEDTRONIC INDICATED THAT THE SENSOR HAD INACCURATE READINGS THAT TRIGGERED THRESHOLD SUSPEND ALARM. THE CUSTOMER¿S BLOOD GLUCOSE WAS 124 MG/DL AND THE SENSOR GLUCOSE WAS 64 MG/DL AT THE TIME OF THE INCIDENT. THE CUSTOMER WAS INFORMED THAT THEIR BLOOD GLUCOSE AND SENSOR GLUCOSE LEVELS WERE NOT IN ACCEPTABLE RANGE. NO HARM REQUIRING MEDICAL INTERVENTION WAS REPORTED. THE SENSOR WILL NOT BE RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 10377343 ↗
• MalfunctionAug 6, 2020Incorrect, Inadequate or Imprecise Result or Readings; Incorrect, Inadequate or Imprecise Result or Readings

  INFORMATION RECEIVED BY MEDTRONIC THE USER REPORTED INACCURATE SENSOR READINGS THAT TRIGGERED A THRESHOLD SUSPEND. THE CUSTOMER¿S BLOOD GLUCOSE WAS 150 MG/DL AND SENSOR GLUCOSE WAS 40 MG/DL AT THE TIME OF THE EVENT, THE DIFFERENCE IS OUTSIDE THE ACCEPTABLE RANGE. NO HARM REQUIRING MEDICAL INTERVENTION WAS REPORTED. THE SENSOR WILL NOT BE RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 10372239 ↗
• InjuryAug 6, 2020Incorrect, Inadequate or Imprecise Result or Readings; Unexpected Therapeutic Results; Incorrect, Inadequate or Imprecise Result or Readings; Unexpected Therapeutic Results

  INFORMATION RECEIVED BY MEDTRONIC THE USER REPORTED INACCURATE SENSOR READINGS THAT TRIGGERED A THRESHOLD SUSPEND. THE CUSTOMER¿S BLOOD GLUCOSE WAS 145 MG/DL AND SENSOR GLUCOSE WAS 45 MG/DL AT THE TIME OF THE EVENT, THE DIFFERENCE IS OUTSIDE THE ACCEPTABLE RANGE. CUSTOMER STATED DIFFERENCE WAS 100 POINTS OFF. NO HARM REQUIRING MEDICAL INTERVENTION WAS REPORTED. THE SENSOR WILL NOT BE RETURNED FOR ANALYSIS.

  Patient problems: Hypoglycemia

  MAUDE report 10371513 ↗
• MalfunctionAug 4, 2020Incorrect, Inadequate or Imprecise Result or Readings; Incorrect, Inadequate or Imprecise Result or Readings

  INFORMATION RECEIVED BY MEDTRONIC THE USER REPORTED INACCURATE SENSOR READINGS THAT TRIGGERED A THRESHOLD SUSPEND. THE CUSTOMER¿S BLOOD GLUCOSE WAS 120 MG/DL AND SENSOR GLUCOSE WAS 66 MG/DL AT THE TIME OF THE EVENT, THE DIFFERENCE WAS OUTSIDE THE ACCEPTABLE RANGE. SENSOR GLUCOSE LEVEL AND BLOOD GLUCOSE LEVEL DIFFERENCE WAS 54 MG/DL. NO HARM REQUIRING MEDICAL INTERVENTION WAS REPORTED. THE SENSOR WILL NOT BE RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 10361132 ↗
• MalfunctionAug 4, 2020Incorrect, Inadequate or Imprecise Result or Readings; Incorrect, Inadequate or Imprecise Result or Readings

  IT WAS REPORTED INACCURATE SENSOR READINGS TRIGGERED A THRESHOLD SUSPEND. THE CUSTOMER¿S BLOOD GLUCOSE WAS 167 MG/DL AND SENSOR GLUCOSE WAS 40 MG/DL AT THE TIME OF THE EVENT, THE DIFFERENCE IS OUTSIDE THE ACCEPTABLE RANGE. SUSPEND ON LOW LIMIT IN SENSOR SETTINGS WAS AT 60 MG/DL. NO HARM REQUIRING MEDICAL INTERVENTION WAS REPORTED. THE SENSOR WILL NOT BE RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 10360672 ↗
• MalfunctionAug 3, 2020Break; Activation Problem; Break; Activation Problem

  INFORMATION RECEIVED BY MEDTRONIC INDICATED THAT THE SENSOR WAS FRACTURED WHILE IN THE BODY. CUSTOMER REPORTED THAT THEY DID NOT RECEIVE MEDICAL TREATMENT AS A RESULT OF THE SENSOR FRACTURING WHILE STILL IN THE BODY. CUSTOMER REPORTED THAT, THE SENSOR WAS STILL IN THE BODY. THE NEEDLE RETRACTING AFTER REMOVING NEEDLE HUB. THE SENSOR WILL BE RETURNED FOR ANALYSIS.

  Patient problems: Foreign Body In Patient

  MAUDE report 10355549 ↗
• MalfunctionAug 3, 2020Incorrect, Inadequate or Imprecise Result or Readings; Unexpected Therapeutic Results; Incorrect, Inadequate or Imprecise Result or Readings; Unexpected Therapeutic Results

  INFORMATION RECEIVED BY MEDTRONIC THE USER REPORTED INACCURATE SENSOR READINGS THAT TRIGGERED A THRESHOLD SUSPEND. THE CUSTOMER¿S BLOOD GLUCOSE WAS 186 MG/DL AND SENSOR GLUCOSE WAS 108 MG/DL AT THE TIME OF THE EVENT, THE DIFFERENCE WAS OUTSIDE THE ACCEPTABLE RANGE. SENSOR GLUCOSE LEVEL AND BLOOD GLUCOSE LEVEL DIFFERENCE WAS 78 MG/DL. NO HARM REQUIRING MEDICAL INTERVENTION WAS REPORTED. THE SENSOR WILL NOT BE RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 10354947 ↗
• MalfunctionJul 31, 2020Fracture; Difficult to Remove; Material Twisted/Bent; Fracture; Difficult to Remove; Material Twisted/Bent

  INFORMATION RECEIVED BY MEDTRONIC INDICATED THAT THE NEEDLE OF SENSOR WAS BROKEN AND BENT. NO HARM REQUIRING MEDICAL INTERVENTION WAS REPORTED. THE SENSOR WILL NOT BE RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 10349186 ↗
• MalfunctionJul 31, 2020Incorrect, Inadequate or Imprecise Result or Readings; Unexpected Therapeutic Results; Incorrect, Inadequate or Imprecise Result or Readings; Unexpected Therapeutic Results

  INFORMATION RECEIVED BY MEDTRONIC THE USER REPORTED INACCURATE SENSOR READINGS THAT TRIGGERED A THRESHOLD SUSPEND. THE CUSTOMER¿S BLOOD GLUCOSE WAS 85 MG/DL AND SENSOR GLUCOSE WAS 40 MG/DL AT THE TIME OF THE EVENT, THE DIFFERENCE IS OUTSIDE THE ACCEPTABLE RANGE. SUSPEND ON LOW LIMIT IN SENSOR SETTINGS WAS AT 70 MG/DL. NO HARM REQUIRING MEDICAL INTERVENTION WAS REPORTED. THE SENSOR WILL NOT BE RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 10348684 ↗
• MalfunctionJul 31, 2020Break; Break

  INFORMATION RECEIVED BY MEDTRONIC INDICATED THAT THE SENSOR WAS HALFWAY HANGING. NO HARM REQUIRING MEDICAL INTERVENTION WAS REPORTED. THE SENSOR WILL NOT BE RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 10348493 ↗
• MalfunctionJul 29, 2020Incorrect, Inadequate or Imprecise Result or Readings; Unexpected Therapeutic Results; Calibration Problem; Incorrect, Inadequate or Imprecise Result or Readings; Unexpected Therapeutic Results; Calibration Problem

  INFORMATION RECEIVED BY MEDTRONIC INDICATED THAT THE SENSOR HAD INACCURATE READINGS THAT TRIGGERED THRESHOLD SUSPEND ALARM. THE CUSTOMER¿S BLOOD GLUCOSE WAS 181 MG/DL AND THE SENSOR GLUCOSE WAS 41 MG/DL. SUSPEND ON LOW LIMIT IN SENSOR SETTINGS WAS 70 MG/DL. INSULIN DELIVERY WAS SUSPENDED DUE TO SENSOR VALUES. NO HARM REQUIRING MEDICAL INTERVENTION WAS REPORTED. THE SENSOR WILL NOT BE RETURNED FOR ANALYSIS.

  Patient problems: Blood Loss

  MAUDE report 10342148 ↗
• MalfunctionJul 27, 2020Incorrect, Inadequate or Imprecise Result or Readings; Unexpected Therapeutic Results; Calibration Problem; Incorrect, Inadequate or Imprecise Result or Readings; Unexpected Therapeutic Results; Calibration Problem

  INFORMATION RECEIVED BY MEDTRONIC THE USER REPORTED INACCURATE SENSOR READINGS THAT TRIGGERED A THRESHOLD SUSPEND. THE CUSTOMER¿S BLOOD GLUCOSE WAS 115 MG/DL AND SENSOR GLUCOSE WAS 44 MG/DL AT THE TIME OF THE EVENT, THE DIFFERENCE WAS OUTSIDE THE ACCEPTABLE RANGE. NO HARM REQUIRING MEDICAL INTERVENTION WAS REPORTED. THE SENSOR WILL NOT BE RETURNED FOR ANALYSIS.

  Patient problems: Blood Loss

  MAUDE report 10325081 ↗
• MalfunctionJul 27, 2020Incorrect, Inadequate or Imprecise Result or Readings; Incorrect, Inadequate or Imprecise Result or Readings

  INFORMATION RECEIVED BY MEDTRONIC THE USER REPORTED INACCURATE SENSOR READINGS THAT TRIGGERED A THRESHOLD SUSPEND. THE CUSTOMER¿S BLOOD GLUCOSE WAS UNDER 68 MG/DL AND SENSOR GLUCOSE WAS UNDER 40 MG/DL AT THE TIME OF THE EVENT, THE DIFFERENCE IS OUTSIDE THE ACCEPTABLE RANGE. SUSPEND ON LOW LIMIT IN SENSOR SETTINGS WAS AT 60 MG/DL. NO HARM REQUIRING MEDICAL INTERVENTION WAS REPORTED. THE SENSOR WILL NOT BE RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 10324767 ↗
• MalfunctionJul 26, 2020Break; Difficult to Remove; Patient Device Interaction Problem; Break; Difficult to Remove; Patient Device Interaction Problem

  INFORMATION RECEIVED BY MEDTRONIC INDICATED THAT THE SENSOR FRACTURED WHILE IN THE BODY. CUSTOMER STATED THAT INSULIN PUMP HAD SENSOR ERROR AND WHEN SHE REMOVED THE SENSOR THE FILLAMENT REMAINED IN LAYSENS SKIN. NO HARM REQUIRING MEDICAL INTERVENTION WAS REPORTED. THE INSULIN PUMP WILL NOT BE RETURNED FOR ANALYSIS.

  Patient problems: Foreign Body In Patient

  MAUDE report 10324609 ↗
• MalfunctionJul 25, 2020Incorrect, Inadequate or Imprecise Result or Readings; Unexpected Therapeutic Results; Incorrect, Inadequate or Imprecise Result or Readings; Unexpected Therapeutic Results

  INFORMATION RECEIVED BY MEDTRONIC INDICATED THAT THE SENSOR HAD INACCURATE READINGS THAT TRIGGERED THRESHOLD SUSPEND ALARM. THE SENSOR GLUCOSE VALUE THAT TRIGGERED THE SUSPEND EVENT WAS 60 MG/DL AND BLOOD GLUCOSE VALUE ASSOCIATED WITH THE TRIGGERED SUSPEND EVENT WAS 208 MG/DL. THE CUSTOMER WAS INFORMED THAT THEIR BLOOD GLUCOSE AND SENSOR GLUCOSE LEVELS WERE NOT IN ACCEPTABLE RANGE. NO HARM REQUIRING MEDICAL INTERVENTION WAS REPORTED. THE SENSOR WILL NOT BE RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 10324266 ↗
• MalfunctionJul 24, 2020Incorrect, Inadequate or Imprecise Result or Readings; Incorrect, Inadequate or Imprecise Result or Readings

  INFORMATION RECEIVED BY MEDTRONIC INDICATED THAT THE CUSTOMER EXPERIENCED SENSOR GLUCOSE VERSUS BLOOD GLUCOSE DIFFERENCES WHERE THE DIFFERENCE WAS OVER 30% AND THE INSULIN PUMP SUSPENDED INSULIN DELIVERY. THE CUSTOMER STATED THE SENSOR GLUCOSE WAS 40 MG/DL WHILE THE BLOOD GLUCOSE WAS 120 MG/DL. NO HARM REQUIRING MEDICAL INTERVENTION WAS REPORTED. TROUBLESHOOTING WAS COMPLETED AND NO OTHER ISSUES WERE FOUND. THE SENSOR WILL NOT BE RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 10319351 ↗
• InjuryJul 23, 2020Fracture; Fracture

  THE CUSTOMER REPORTED VIA PHONE CALL THAT THEY WERE EXPERIENCING¿HIGH¿BLOOD¿GLUCOSE AND THE SENSOR NEEDLE WAS BROKEN. ¿BLOOD¿GLUCOSE¿LEVEL AT THE TIME OF THE INCIDENT WAS ¿415¿MG/DL. THE CUSTOMER STATED THAT THE SENSOR WAS RETRACTED AND THE NEEDLE WAS BROKEN AFTER REMOVAL. THE CUSTOMER DID NOT RECEIVE MEDICAL TREATMENT AS A RESULT OF THE NEEDLE FRACTURING WHILE STILL IN THE BODY. CUSTOMER WAS NOT USING AUTO MODE AT THE TIME OF INCIDENCE. THE INSULIN PUMP AND SENSOR WILL NOT BE RETURNED FOR ANALYSIS.

  Patient problems: Foreign Body In Patient; Hyperglycemia

  MAUDE report 10313005 ↗
• MalfunctionJul 22, 2020Incorrect, Inadequate or Imprecise Result or Readings; Incorrect, Inadequate or Imprecise Result or Readings

  INFORMATION RECEIVED BY MEDTRONIC INDICATED THAT THE SENSOR HAD INACCURATE READINGS THAT TRIGGERED THRESHOLD SUSPEND. BLOOD GLUCOSE WAS 97 MG/DL. THERE IS A DIFFERENCE IN VALUE OF 37 POINTS BETWEEN SENSOR GLUCOSE AND BLOOD GLUCOSE. NO HARM REQUIRING MEDICAL INTERVENTION WAS REPORTED. THE PRODUCT WILL NOT RETURN FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 10306904 ↗
• MalfunctionJul 21, 2020Fracture; Patient Device Interaction Problem; Fracture; Patient Device Interaction Problem

  INFORMATION RECEIVED BY MEDTRONIC INDICATED THAT THE SENSOR PIECE WAS BROKEN IN THE STOMACH. THE CUSTOMER STATED THAT THE SENSOR WAS NOT STAYING IN AND THE TAPE WAS NOT STICKING. THE CUSTOMER DECLINED TROUBLESHOOTING FOR BLOOD AT THE SITE, FOR THE NEEDLE BROKE, AND FOR TAPE NOT STICKING. NO HARM REQUIRING MEDICAL INTERVENTION WAS REPORTED. THE SENSOR WILL NOT BE RETURNED FOR ANALYSIS.

  Patient problems: Blood Loss; Foreign Body In Patient

  MAUDE report 10306175 ↗
• MalfunctionJul 20, 2020Difficult to Remove; Patient Device Interaction Problem; Difficult to Remove; Patient Device Interaction Problem

  INFORMATION RECEIVED BY MEDTRONIC INDICATED THAT NEEDLE WAS BREAK DURING INSERTION. CUSTOMER STATED THAT THE INTRODUCER NEEDLE WAS HARD TO REMOVED. NO HARM REQUIRING MEDICAL INTERVENTION WAS REPORTED. THE SENSOR WILL NOT BE RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 10295377 ↗
• MalfunctionJul 20, 2020Incorrect, Inadequate or Imprecise Result or Readings; Incorrect, Inadequate or Imprecise Result or Readings

  INFORMATION RECEIVED BY MEDTRONIC THE USER REPORTED INACCURATE SENSOR READINGS THAT TRIGGERED A THRESHOLD SUSPEND. THE CUSTOMER¿S BLOOD GLUCOSE WAS 120 MG/DL AND SENSOR GLUCOSE WAS 75 MG/DL AT THE TIME OF THE EVENT, THE DIFFERENCE IS OUTSIDE THE ACCEPTABLE RANGE. SUSPEND ON LOW LIMIT IN SENSOR SETTINGS WAS AT 75 MG/DL. NO HARM REQUIRING MEDICAL INTERVENTION WAS REPORTED. THE SENSOR WILL NOT BE RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 10294699 ↗

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-1739-2026 · Feb 13, 2026 · Open, Classified
  MiniMed 670G Insulin Pump (MMT-1760, MMT-1761, MMT-1762, MMT-1780, 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-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-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-0003-2025 · Jul 31, 2024 · Open, Classified
  MiniMed Insulin Pump Device. MiniMed 670G, REF: MMT-1580, MMT-1581, MMT-1582, MMT-1780, MMT-1781, MMT-1782, MMT-1740, MMT-1741, MMT-1742, MMT-1760, MMT-1761, MMT-1762; MiniMed 770G
• 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-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.
• Z-2605-2017 · May 8, 2017 · Terminated
  MiniMed 670G Insulin Infusion Pump, Catalog No. MMT-1580, MMT-1780, MMT-1782, MMT-1760.