Guardian ™ Sensor (3) MMT-7020A (UDI 00763000017552)Recalls & reported problems

Summary

The FDA's MAUDE database contains 329 adverse event reports that list this exact device (DI 00763000017552), received between Jan 22, 2018 and Jan 31, 2019 — classified as 182 injuries, 147 malfunctions.

The most frequently reported specific device problem is “Device Displays Incorrect Message” (72 reports).

22 other recalls cover devices cleared under the same FDA submission (P150001, 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 16, 2026.

Most reported problems

Recent adverse event reports

The 25 most recent of 329 reports, in the reporter's own words as published by the FDA.

• InjuryJan 31, 2019Incorrect, Inadequate or Imprecise Result or Readings; Calibration Problem; Incorrect, Inadequate or Imprecise Result or Readings; Calibration Problem

  THE CUSTOMER REPORTED VIA PHONE CALL THE SENSOR HAD INACCURATE READINGS THAT TRIGGERED THRESHOLD SUSPEND ALARM. THE CUSTOMER¿S BLOOD GLUCOSE WAS 168 MG/DL AND THE SENSOR GLUCOSE WAS 72 MG/DL AT THE TIME OF THE INCIDENT. SENSOR GLUCOSE VALUE THAT TRIGGERED SUSPEND EVENT WAS 74 MG/DL. THE DIFFERENCE BETWEEN THE SENSOR GLUCOSE LEVEL AND BLOOD GLUCOSE LEVEL WAS 96 MG/DL THE CUSTOMER WAS INFORMED THAT THEIR BLOOD GLUCOSE AND SENSOR GLUCOSE LEVELS WERE NOT IN ACCEPTABLE RANGE. THE SENSOR WILL NOT BE RETURNED FOR ANALYSIS.

  Patient problems: Blood Loss; Hypoglycemia

  MAUDE report 8294059 ↗
• InjuryJan 7, 2019Fracture; Incorrect, Inadequate or Imprecise Result or Readings; Calibration Problem; Fracture; Incorrect, Inadequate or Imprecise Result or Readings; Calibration Problem

  THE CUSTOMER REPORTED VIA PHONE CALL THAT SENSOR CANNULA BROKE OFF IN HIS BODY AND IS STILL IN THE BODY AS WELL AS A SENSOR THAT HAD SENSOR UPDATING AND CHANGE SENSOR ALARM. BLOOD GLUCOSE WAS UNKNOWN. THE DEVICE WILL BE RETURNED FOR ANALYSIS.

  Patient problems: Blood Loss; Foreign Body In Patient

  MAUDE report 8221502 ↗
• MalfunctionDec 28, 2018Incorrect, Inadequate or Imprecise Result or Readings; Incorrect, Inadequate or Imprecise Result or Readings

  THE CUSTOMER REPORTED VIA PHONE CALL THAT THE SENSOR HAD INACCURATE READINGS THAT TRIGGERED THRESHOLD SUSPEND ALARM. THE CUSTOMER¿S BLOOD GLUCOSE WAS 280 MG/DL AND THE SENSOR GLUCOSE WAS 61 MG/DL. INSULIN DELIVERY WAS SUSPENDED DUE TO SENSOR GLUCOSE VALUES. THE CUSTOMER WAS INFORMED THAT THEIR BLOOD GLUCOSE AND SENSOR GLUCOSE LEVELS WERE NOT IN ACCEPTABLE RANGE. THE SENSOR WILL NOT RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 8202072 ↗
• MalfunctionDec 14, 2018Incorrect, Inadequate or Imprecise Result or Readings; Calibration Problem; Incorrect, Inadequate or Imprecise Result or Readings; Calibration Problem

  THE CUSTOMER REPORTED VIA PHONE CALL THE SENSOR HAD INACCURATE READINGS THAT TRIGGERED THRESHOLD SUSPEND ALARM. THE CUSTOMER¿S BLOOD GLUCOSE VALUES WAS 95 MG/DL, 315 MG/DL, 95 MG/DL AND THE SENSOR GLUCOSE WAS 57 MG/DL, 276 MG/DL. INSULIN DELIVERY WAS SUSPENDED DUE TO SENSOR VALUES. SENSOR VALUE THAT TRIGGERED THE SUSPEND EVENT WAS 95 MG/DL. SUSPEND ON LOW LIMIT IN SENSOR SETTINGS WAS 57 MG/DL. THE CUSTOMER WAS INFORMED THAT THEIR BLOOD GLUCOSE AND SENSOR GLUCOSE LEVELS WERE NOT IN ACCEPTABLE RANGE. THE SENSOR WILL BE RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 8163390 ↗
• MalfunctionNov 28, 2018Incorrect, Inadequate or Imprecise Result or Readings; Calibration Problem; Patient Device Interaction Problem; Incorrect, Inadequate or Imprecise Result or Readings; Calibration Problem; Patient Device Interaction Problem

  THE CUSTOMER REPORTED VIA PHONE CALL THAT THE SENSOR HAD INACCURATE READINGS THAT TRIGGERED THRESHOLD SUSPEND ALARM. THE CUSTOMER¿S BLOOD GLUCOSE WAS 101 MG/DL AND THE SENSOR GLUCOSE WAS 92 MG/DL. INSULIN DELIVERY WAS SUSPENDED DUE TO SENSOR VALUES. THE CUSTOMER WAS INFORMED THAT THEIR BLOOD GLUCOSE AND SENSOR GLUCOSE LEVELS WERE NOT IN ACCEPTABLE RANG. THE SENSOR WILL BE RETURNED FOR ANALYSIS.

  Patient problems: Rash

  MAUDE report 8113405 ↗
• MalfunctionNov 16, 2018Break; Incorrect, Inadequate or Imprecise Result or Readings; Calibration Problem; Break; Incorrect, Inadequate or Imprecise Result or Readings; Calibration Problem

  CUSTOMER'S PARENT REPORTED VIA PHONE CALL SENSOR ANOMALY. CUSTOMER'S BLOOD GLUCOSE LEVEL WAS 222 MG/DL. CUSTOMER ADVISED THEY EXPERIENCED IRRITATION ISSUES WITH THEIR SENSOR. CUSTOMER WAS ADVISED TO RETURN THE SENSOR FOR ANALYSIS.

  Patient problems: Inflammation; Skin Erosion; Skin Inflammation; Skin Irritation

  MAUDE report 8076798 ↗
• MalfunctionNov 14, 2018Break; Patient Device Interaction Problem; Break; Patient Device Interaction Problem

  THE CUSTOMER REPORTED THAT THE SENSOR NEEDLE WAS BROKEN WHEN PEELING BACK. THE CUSTOMER'S BLOOD GLUCOSE WAS UNKNOWN AT THE TIME OF INCIDENT. THE SENSOR WILL BE RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 8071240 ↗
• MalfunctionOct 25, 2018Incorrect, Inadequate or Imprecise Result or Readings; Incorrect, Inadequate or Imprecise Result or Readings

  THE CUSTOMER REPORTED VIA PHONE CALL THE SENSOR HAD INACCURATE READINGS THAT TRIGGERED THRESHOLD SUSPEND ALARM. THE CUSTOMER¿S BLOOD GLUCOSE WAS 96 MG/DL AND THE SENSOR GLUCOSE WAS 61 MG/DL. INSULIN DELIVERY WAS SUSPENDED DUE TO SENSOR VALUES. SENSOR VALUE THAT TRIGGERED THE SUSPEND EVENT WAS 65 MG/DL. SUSPEND ON LOW LIMIT IN SENSOR SETTINGS WAS 65 MG/DL. THE CUSTOMER WAS INFORMED THAT THEIR BLOOD GLUCOSE AND SENSOR GLUCOSE LEVELS WERE NOT IN ACCEPTABLE RANGE. THE SENSOR WILL BE RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 8004194 ↗
• MalfunctionOct 16, 2018Incorrect, Inadequate or Imprecise Result or Readings; Incorrect, Inadequate or Imprecise Result or Readings

  THE CUSTOMER REPORTED VIA PHONE CALL THE SENSOR HAD INACCURATE READINGS THAT TRIGGERED THRESHOLD SUSPEND ALARM. THE CUSTOMER¿S BLOOD GLUCOSE WAS 290 MG/DL AND THE SENSOR GLUCOSE WAS 110 MG/DL. INSULIN DELIVERY WAS SUSPENDED DUE TO SENSOR VALUES. SENSOR VALUE THAT TRIGGERED THE SUSPEND EVENT WAS 65 MG/DL. SUSPEND ON LOW LIMIT IN SENSOR SETTINGS WAS 70 MG/DL. THE CUSTOMER WAS INFORMED THAT THEIR BLOOD GLUCOSE AND SENSOR GLUCOSE LEVELS WERE NOT IN ACCEPTABLE RANGE. THE SENSOR WILL NOT BE RETURNED FOR ANALYSIS.

  Patient problems: Itching Sensation

  MAUDE report 7968496 ↗
• MalfunctionSep 25, 2018Incorrect, Inadequate or Imprecise Result or Readings; Incorrect, Inadequate or Imprecise Result or Readings

  THE CUSTOMER REPORTED VIA PHONE CALL THAT THE SENSOR HAD INACCURATE READINGS THAT TRIGGERED THRESHOLD SUSPEND ALARM. THE CUSTOMER¿S BLOOD GLUCOSE WAS 132 MG/DL AND THE SENSOR GLUCOSE WAS 88 MG/DL. INSULIN DELIVERY WAS SUSPENDED DUE TO SENSOR GLUCOSE VALUES. THE CUSTOMER WAS INFORMED THAT THEIR BLOOD GLUCOSE AND SENSOR GLUCOSE LEVELS WERE NOT IN ACCEPTABLE RANGE. THE SENSOR WILL RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 7904527 ↗
• MalfunctionSep 17, 2018Incorrect, Inadequate or Imprecise Result or Readings; Incorrect, Inadequate or Imprecise Result or Readings

  THE CUSTOMER'S PARENT REPORTED VIA PHONE CALL THE SENSOR HAD INACCURATE READINGS THAT TRIGGERED THE INSULIN PUMP TO TURN OFF. CUSTOMER¿S BLOOD GLUCOSE WAS 130-140 MG/DL AND THE SENSOR GLUCOSE WAS BELOW 70 MG/DL AT THE TIME OF THE INCIDENT. CUSTOMER WOULD DO CORRECTION THROUGH THE INSULIN PUMP. EXPLAINED TO CUSTOMER HOW TO NAVIGATE THE DEVICE OUT OF SUSPEND WHEN IT SUSPENDS FOR A LOW AND WHEN THE CENTER BUTTON IS PRESSED IT WILL NOT RESPOND. THE SENSOR WILL NOT BE RETURNED FOR ANALYSIS.

  Patient problems: Hyperglycemia

  MAUDE report 7882080 ↗
• MalfunctionSep 11, 2018Patient Device Interaction Problem; Patient Device Interaction Problem

  CUSTOMER REPORTED VIA PHONE CALL ON (B)(6) 2018 THAT THE INSULIN PUMP WAS HAVING ISSUES WITH SENSOR GLUCOSE VERSUS BLOOD GLUCOSE LEVELS. CUSTOMER'S BLOOD GLUCOSE LEVEL WAS OVER 203MG/DL AND THE SENSOR GLUCOSE READING WAS 44MG/DL THAT TRIGGERED THE INSULIN PUMP TO SUSPEND INSULIN DELIVERY. THE THRESHOLD LOW SUSPEND LIMIT WAS 80-85 MG/DL. TROUBLESHOOTING DID NOT RESOLVE ISSUE. THE SENSOR WAS NOT RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 7866615 ↗
• InjurySep 11, 2018Incorrect, Inadequate or Imprecise Result or Readings; Incorrect, Inadequate or Imprecise Result or Readings

  THE CUSTOMER REPORTED VIA PHONE CALL THAT THE SENSOR HAD INACCURATE READINGS THAT TRIGGERED THRESHOLD SUSPEND ALARM. THE CUSTOMER¿S BLOOD GLUCOSE WAS 278 MG/DL AND THE SENSOR GLUCOSE WAS 40 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. THE SENSOR WILL NOT BE RETURNED FOR ANALYSIS.

  Patient problems: Hyperglycemia

  MAUDE report 7866387 ↗
• MalfunctionSep 7, 2018Unexpected Therapeutic Results; Unexpected Therapeutic Results

  CUSTOMER REPORTED VIA PHONE CALL THE SENSOR HAD INACCURATE READINGS THAT TRIGGERED THE THRESHOLD SUSPEND ALARM. THE CUSTOMER¿S BLOOD GLUCOSE WAS 139 MG/DL AND THE SENSOR GLUCOSE WAS 85 MG/DL AT THE TIME OF THE INCIDENT. CUSTOMER WAS INFORMED THAT THEIR BLOOD GLUCOSE AND SENSOR GLUCOSE LEVELS WERE NOT IN ACCEPTABLE RANGE. CUSTOMER WAS ADVISED A REPLACEMENT SENSOR WOULD BE SENT OUT.

  Patient problems: Hyperglycemia

  MAUDE report 7856384 ↗
• InjurySep 4, 2018No Apparent Adverse Event; No Apparent Adverse Event

  CUSTOMER REPORTED VIA PHONE CALL THAT THEY EXPERIENCED A LOW BLOOD GLUCOSE. CUSTOMER¿S BLOOD GLUCOSE LEVEL WAS 47 MG/DL. CUSTOMER DECLINE TROUBLESHOOTING FOR LOW BLOOD GLUCOSE. THE CUSTOMER TREATED WITH GLUCOSE AND CARBOHYDRATES. THE PRODUCT WILL NOT BE RETURN FOR THE ANALYSIS.

  Patient problems: Hypoglycemia

  MAUDE report 7841358 ↗
• MalfunctionAug 27, 2018Calibration Problem; Calibration Problem

  THE CUSTOMER REPORTED VIA PHONE CALL THAT THEY EXPERIENCED INACCURATE READINGS AND TRIGGERED THRESHOLD SUSPEND. THE CUSTOMER'S BLOOD GLUCOSE WAS 190 MG/DL AND SENSOR GLUCOSE WAS 40 MG/DL AT THE TIME OF INCIDENT WHEN IT TRIGGERED THRESHOLD SUSPEND. THE SENSOR WILL BE RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 7816170 ↗
• MalfunctionAug 27, 2018Incorrect, Inadequate or Imprecise Result or Readings; Incorrect, Inadequate or Imprecise Result or Readings

  THE CUSTOMER REPORTED VIA PHONE CALL THE SENSOR HAD INACCURATE READINGS THAT TRIGGERED THRESHOLD SUSPEND ALARM. THE CUSTOMER¿S BLOOD GLUCOSE WAS 150 MG/DL AND THE SENSOR GLUCOSE WAS 83 MG/DL. INSULIN DELIVERY WAS SUSPENDED DUE TO SENSOR VALUES. THE CUSTOMER WAS INFORMED THAT THEIR BLOOD GLUCOSE AND SENSOR GLUCOSE LEVELS WERE NOT IN ACCEPTABLE RANGE. SENSOR GLUCOSE VALUE THAT TRIGGERED THE SUSPEND EVENT WAS 40 MG/DL. THE PRODUCT WILL NOT BE RETURNED FOR ANALYSIS.

  Patient problems: Hyperglycemia

  MAUDE report 7816100 ↗
• MalfunctionAug 24, 2018Calibration Problem; Calibration Problem

  THE CUSTOMER REPORTED VIA PHONE CALL THAT THEY EXPERIENCED INACCURATE READINGS AND TRIGGERED THRESHOLD SUSPEND. THE CUSTOMER'S BLOOD GLUCOSE WAS 73 MG/DL AND SENSOR GLUCOSE WAS 43 MG/DL AT THE TIME OF INCIDENT WHEN IT TRIGGERED THRESHOLD SUSPEND. THE CUSTOMER'S BLOOD GLUCOSE WAS 83 MG/DL AT THE TIME OF CALL. THE SENSOR WAS RETURNED FOR ANALYSIS.

  Patient problems: Blood Loss

  MAUDE report 7815374 ↗
• MalfunctionAug 24, 2018Calibration Problem; Calibration Problem

  THE CUSTOMER REPORTED VIA PHONE CALL THAT THEY EXPERIENCED INACCURATE READINGS AND TRIGGERED THRESHOLD SUSPEND. THE CUSTOMER'S BLOOD GLUCOSE WAS 120 MG/DL AND SENSOR GLUCOSE WAS 55 MG/DL AT THE TIME OF INCIDENT WHEN IT TRIGGERED THRESHOLD SUSPEND. THE SENSOR WAS RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 7815364 ↗
• MalfunctionAug 24, 2018Calibration Problem; Calibration Problem

  THE CUSTOMER REPORTED VIA PHONE CALL THAT THEY EXPERIENCED INACCURATE READINGS AND TRIGGERED THRESHOLD SUSPEND. THE CUSTOMER'S BLOOD GLUCOSE WAS 186 MG/DL AND SENSOR GLUCOSE WAS 60 MG/DL AT THE TIME OF INCIDENT WHEN IT TRIGGERED THRESHOLD SUSPEND. THE SENSOR WILL BE RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 7815312 ↗
• MalfunctionAug 24, 2018Incorrect, Inadequate or Imprecise Result or Readings; Incorrect, Inadequate or Imprecise Result or Readings

  THE CUSTOMER REPORTED VIA PHONE CALL THAT THEY EXPERIENCED INACCURATE READINGS AND TRIGGERED THRESHOLD SUSPEND. THE CUSTOMER'S BLOOD GLUCOSE WAS 120 MG/DL AND SENSOR GLUCOSE WAS 48 MG/DL AT THE TIME OF INCIDENT WHEN IT TRIGGERED THRESHOLD SUSPEND. THE SENSOR WILL BE RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 7815295 ↗
• MalfunctionAug 23, 2018Incorrect, Inadequate or Imprecise Result or Readings; Incorrect, Inadequate or Imprecise Result or Readings

  THE CUSTOMER REPORTED VIA PHONE CALL THAT THEY EXPERIENCED INACCURATE READINGS AND TRIGGERED THRESHOLD SUSPEND. THE CUSTOMER'S BLOOD GLUCOSE WAS 160 MG/DL AND SENSOR GLUCOSE WAS 70 MG/DL AT THE TIME OF INCIDENT WHEN IT TRIGGERED THRESHOLD SUSPEND. THE SENSOR WILL BE RETURNED FOR ANALYSIS.

  Patient problems: Hyperglycemia

  MAUDE report 7811085 ↗
• InjuryAug 21, 2018No Apparent Adverse Event; No Apparent Adverse Event

  CUSTOMER REPORTED VIA PHONE CALL ON (B)(6) 2018 THAT HER INSULIN PUMP AND SENSOR WAS UNABLE TO CALIBRATE. CUSTOMER REPORTED A HIGH BLOOD GLUCOSE LEVEL OF 424 MG/DL AND TREATED WITH INSULIN PUMP. BLOOD GLUCOSE LEVEL AT THE TIME OF THE CALL WAS 280 MG/DL. TROUBLESHOOTING OCCURRED BUT ISSUE REMAINS UNRESOLVED. AUTOMODE FEATURE WAS ENGAGED AT THE TIME OF THE INCIDENT. SENSOR WILL BE RETURNED FOR ANALYSIS.

  Patient problems: Hyperglycemia

  MAUDE report 7803518 ↗
• MalfunctionAug 21, 2018No Apparent Adverse Event; No Apparent Adverse Event

  THE CUSTOMER REPORTED VIA PHONE CALL THE SENSOR HAD INACCURATE READINGS THAT TRIGGERED THRESHOLD SUSPEND ALARM. THE CUSTOMER¿S BLOOD GLUCOSE WAS 150 MG/DL AND THE SENSOR GLUCOSE WAS 54 MG/DL AT THE TIME OF THE INCIDENT. CUSTOMER WAS ADVISED THAT THE SENSOR GLUCOSE AND BLOOD GLUCOSE READINGS WILL BE CLOSE BUT RARELY MATCH DUE TO HOW GLUCOSE TRAVELS IN THE BODY. THE CUSTOMER WAS INFORMED THAT THEIR BLOOD GLUCOSE AND SENSOR GLUCOSE LEVELS WERE NOT IN ACCEPTABLE RANGE. THE CUSTOMER WAS ADVISED THAT SENSOR IS BEING REPLACED. THE SENSOR WILL NOT BE RETURNED FOR ANALYSIS. FRN RESERVOIR UNKNOWN. UNOMEDICAL INFUSION SET.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 7802536 ↗
• MalfunctionAug 20, 2018Unexpected Therapeutic Results; Unexpected Therapeutic Results

  THE CUSTOMER REPORTED VIA PHONE CALL THE SENSOR HAD INACCURATE READINGS THAT TRIGGERED THRESHOLD SUSPEND ALARM. THE CUSTOMER¿S BLOOD GLUCOSE WAS 104 MG/DL AND THE SENSOR GLUCOSE WAS 69 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. THE SENSOR WILL BE RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 7796450 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under P150001, 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-1740-2026 · Feb 13, 2026 · Open, Classified
  MiniMed 630G Insulin Pump (MMT-1714, MMT-1715, MMT-1754, MMT-1755)
• 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-1739-2026 · Feb 13, 2026 · Open, Classified
  MiniMed 670G Insulin Pump (MMT-1760, MMT-1761, MMT-1762, MMT-1780, MMT-1781, MMT-1782)
• 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-1259-2025 · Jan 31, 2025 · Open, Classified
  MiniMed insulin pump, REF: 630G (MMT-1714, MMT-1715, MMT-1754, MMT-1755)
• 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-0001-2025 · Jul 31, 2024 · Open, Classified
  MiniMed 630G Insulin Pump, REF: MMT-1515, MMT-1714, MMT-1715, MMT-1754, MMT-1755; MiniMed 700G Insulin Pump, REF: MMT-1800, MMT-1801, MMT-1805, MMT-1850, MMT-1851
• 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-18
• 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
• Z-0517-2021 · Apr 30, 2020 · Open, Classified
  MiniMed 630G with SmartGuard, insulin pump, Ref/Model # MMT-1754K, MMT-1714K, MMT-1755K - Product Usage: intended for continuous delivery of basal insulin (at user selectable rate
• 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

…and 7 more.