MiniMed® 630G MMT-1715KL (UDI 00763000316655)Recalls & reported problems

Summary

The FDA's MAUDE database contains 266 adverse event reports that list this exact device (DI 00763000316655), received between Dec 9, 2019 and Mar 9, 2023 — classified as 106 injuries, 160 malfunctions.

The most frequently reported specific device problem is “No Display/Image” (53 reports).

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

21 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 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-1748-2026 · 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-0001-2025 · Root cause: Device Design · Recall details · FDA record ↗

Most reported problems

Recent adverse event reports

The 25 most recent of 266 reports, in the reporter's own words as published by the FDA.

• MalfunctionMar 9, 2023Battery Problem; Battery Problem

  INFORMATION RECEIVED BY MEDTRONIC INDICATED THAT THE CUSTOMER RECEIVED REPLACE BATTERY NOW ALERT. NO HARM REQUIRING MEDICAL INTERVENTION WAS REPORTED. TROUBLESHOOTING WAS PERFORMED AND CUSTOMER CONFIRMED THERE WAS NOT LOOSE, CRACKED OR DAMAGED BATTERY CAP. CUSTOMER WAS ALSO NOT USED THE SUSPEND BEFORE LOW OR SUSPEND ON LOW CGM FEATURE WITH MINIMED 630G PUMP BUT IT ALARMED LESS THAN 8 HRS. FROM LOW BATTERY ALERT TO REPLACE BATTERY NOW ALARM. CUSTOMER WILL DISCONTINUE TO USE THE DEVICE. THE PUMP WILL BE RETURNED FOR ANALYSIS.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 16510415 ↗
• MalfunctionJun 26, 2022No Display/Image; Material Integrity Problem

  MEDTRONIC RECEIVED INFORMATION THAT BLANK DISPLAY, 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 14823992 ↗
• MalfunctionMay 8, 2022Human-Device Interface Problem; Human-Device Interface Problem

  IT WAS IDENTIFIED THAT THE CUSTOMER¿S BASAL PROGRAMMING WAS UNKNOWN. CUSTOMER WAS HIGH UP TO 328 MG/DL. CUSTOMER DID NOT HAD BASAL SETUP. THE DEVICE WILL NOT BE RETURNED.

  Patient problems: Hyperglycemia

  MAUDE report 14332091 ↗
• MalfunctionApr 28, 2022Human-Device Interface Problem; Human-Device Interface Problem

  IT WAS IDENTIFIED THAT THE CUSTOMER'S BASAL PROGRAMMING WAS UNKNOWN. THE CUSTOMER REPORTED THAT THEY HAD NOT BEEN GETTING HER BASAL RATES AND THE INSULIN PUMP WAS NOT PROGRAMMED. THE CUSTOMER'S BLOOD GLUCOSE AT THE TIME OF THE EVENT WAS 300 MG/DL. THE CUSTOMER DECLINED FURTHER TROUBLESHOOTING. THE INSULIN PUMP WILL NOT BE RETURNED FOR ANALYSIS.

  Patient problems: Hyperglycemia

  MAUDE report 14240276 ↗
• MalfunctionApr 19, 2022Obstruction of Flow; Human-Device Interface Problem; Obstruction of Flow; Human-Device Interface Problem

  IT WAS IDENTIFIED THAT THE USER WAS NOT AWARE OR HAD FORGOTTEN HIS BASAL PROGRAMMING. THE CUSTOMER REPORTED THAT THEY GOT INSULIN FLOW BLOCKED ALARM. THE BLOOD GLUCOSE LEVEL WAS 211MG/DL. CUSTOMER TOOK BOLUS AND AFTER 2 HOURS BLOOD GLUCOSE WAS 200 MG/DL. THE DEVICE WILL NOT BE RETURNED FOR ANALYSIS.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 14139647 ↗
• MalfunctionSep 14, 2021Break; Material Integrity Problem; Break; Material Integrity Problem

  INFORMATION RECEIVED BY MEDTRONIC INDICATED THAT THE INSULIN PUMP HAD A MISSING RESERVOIR CAP. NO HARM REQUIRING MEDICAL INTERVENTION WAS REPORTED. THE INSULIN PUMP WILL BE NOT RETURNED FOR ANALYSIS.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 12467149 ↗
• MalfunctionNov 10, 2020Battery Problem; Power Problem; Battery Problem; Power Problem

  INFORMATION RECEIVED BY MEDTRONIC INDICATED THAT INSULIN PUMP RECEIVED LOW BATTERY ALARM AND REPLACE BATTERY NOW ALARM. CUSTOMER STATED THAT BATTERY CAP WAS NOT LOOSEN, CRACKED OR DAMAGED. NO HARM REQUIRING MEDICAL INTERVENTION WAS REPORTED. THE INSULIN PUMP WILL BE RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 10814841 ↗
• MalfunctionSep 8, 2020Power Problem; Power Problem

  INFORMATION RECEIVED BY MEDTRONIC INDICATED THAT INSULIN PUMP GOT BATTERY FAILED ALERT. NO HARM REQUIRING MEDICAL INTERVENTION WAS REPORTED. THE CUSTOMER WAS ASSISTED WITH TROUBLESHOOTING. THE DEVICE WILL BE RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 10500744 ↗
• MalfunctionSep 7, 2020Patient Device Interaction Problem; Patient Device Interaction Problem

  INFORMATION RECEIVED BY MEDTRONIC INDICATED THAT THE RESERVOIR PART HAD CRACK. CUSTOMER STATED THE RESERVOIR LIP RING DID NOT SHOW SIGNS OF DAMAGE. NO HARM REQUIRING MEDICAL INTERVENTION WAS REPORTED. THE INSULIN PUMP WILL BE RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 10498733 ↗
• MalfunctionSep 4, 2020Battery Problem; Adverse Event Without Identified Device or Use Problem; Battery Problem; Adverse Event Without Identified Device or Use Problem

  INFORMATION RECEIVED BY MEDTRONIC INDICATED THAT INSULIN PUMP HAD LOW BATTERY ALERT AND INSERT BATTERY ALERT. CUSTOMER STATED THAT BATTERY DID NOT LAST MORE THAN 1 WEEK. NO HARM REQUIRING MEDICAL INTERVENTION WAS REPORTED. THE CUSTOMER WAS ASSISTED WITH TROUBLESHOOTING. THE DEVICE WILL BE RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 10492636 ↗
• MalfunctionAug 24, 2020Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  INFORMATION RECEIVED BY MEDTRONIC INDICATED THAT THE INSULIN PUMP WAS DELIVERING LOW INSULIN. CUSTOMER STATED THAT BLOOD GLUCOSE 280 MG/DL WHICH WAS NOT GOING DOWN. CUSTOMER DECLINED TROUBLESHOOTING FOR HIGH BLOOD GLUCOSE LEVEL NO HARM REQUIRING MEDICAL INTERVENTION WAS REPORTED. THE INSULIN PUMP WILL BE RETURNED FOR ANALYSIS.

  Patient problems: Hyperglycemia

  MAUDE report 10446671 ↗
• MalfunctionAug 23, 2020No Display/Image; Moisture or Humidity Problem; Patient Device Interaction Problem; No Display/Image; Moisture or Humidity Problem; Patient Device Interaction Problem

  INFORMATION RECEIVED BY MEDTRONIC INDICATED THAT THE INSULIN PUMP HAD A BLANK DISPLAY. CUSTOMER STATED THE BATTERY WAS CHANGED, BUT THE ISSUE WAS NOT RESOLVED. CUSTOMER STATED THAT INSULIN PUMP EXPOSED TO MOISTURE. NO HARM REQUIRING MEDICAL INTERVENTION WAS REPORTED. THE INSULIN PUMP WILL BE RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 10440670 ↗
• MalfunctionAug 21, 2020Patient Device Interaction Problem; Patient Device Interaction Problem

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

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 10436390 ↗
• MalfunctionAug 17, 2020Device Alarm System; Device Alarm System

  INFORMATION RECEIVED BY MEDTRONIC INDICATED THAT THE INSULIN PUMP DID NOT ALARM HER LAST NIGHT WHEN SHE GOT THE LOW BATTERY ALARM AND THE REWINDING WAS TOO LOUD. CUSTOMER STATED THEY SAW MISSING SEGMENTS DURING THE SELF TEST. CUSTOMER STATED THE SELF TEST PASSED. NO HARM REQUIRING MEDICAL INTERVENTION WAS REPORTED. THE INSULIN PUMP WILL BE RETURNED FOR ANALYSIS.

  Patient problems: Hyperglycemia

  MAUDE report 10412395 ↗
• InjuryAug 12, 2020Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  CUSTOMER REPORTED VIA PHONE CALL THAT THEY EXPERIENCED HIGH BLOOD GLUCOSE. THE CUSTOMER BLOOD GLUCOSE LEVEL WAS 560 MG/DL AT THE TIME OF INCIDENT AND CURRENT BLOOD GLUCOSE VALUE WAS 466 MG/DL. CUSTOMER WAS USING INSULIN PUMP SYSTEM WITHIN 48 HOURS OF REPORTED HIGH BLOOD GLUCOSE EVENT. CUSTOMER REPORTED THAT AUTO MODE FEATURE WAS NOT ACTIVE AT TIME OF HIGH BLOOD GLUCOSE EVENT. CUSTOMER TREATED WITH SHOT. THE CUSTOMER WAS ASSISTED WITH TROUBLESHOOTING AND DECLINED FOR HIGH BLOOD GLUCOSE. THE INSULIN PUMP WILL NOT BE RETURNED FOR ANALYSIS.

  Patient problems: Hyperglycemia

  MAUDE report 10395341 ↗
• MalfunctionAug 12, 2020No Display/Image; No Display/Image

  INFORMATION RECEIVED BY MEDTRONIC INDICATED THAT THE INSULIN PUMP HAD A BLANK DISPLAY. THE CUSTOMER STATED THE DISPLAY DID NOT RETURN EVEN AFTER A BATTERY CHANGE. NO HARM REQUIRING MEDICAL INTERVENTION WAS REPORTED. TROUBLESHOOTING WAS COMPLETED BUT DID NOT RESOLVE THE ISSUE. THE INSULIN PUMP WILL BE RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 10395107 ↗
• MalfunctionAug 12, 2020Device Difficult to Program or Calibrate; Device Difficult to Program or Calibrate

  INFORMATION RECEIVED BY MEDTRONIC INDICATED THAT THE INSULIN PUMP HAD KEYPAD ANOMALY. THE CUSTOMER STATED THAT, THE BUTTONS WERE UNRESPONSSIVE. IT WAS OFF FOR COUPLE OF DAYS AND WHEN SHE TRIED TO TURN IT BACK ON BUTTONS WERE NOT RESPONDING. NO HARM REQUIRING MEDICAL INTERVENTION WAS REPORTED. THE INSULIN PUMP WILL NOT BE RETURNED FOR ANALYSIS.

  Patient problems: Hyperglycemia

  MAUDE report 10394709 ↗
• InjuryAug 11, 2020Device Alarm System; Device Alarm System

  THE CUSTOMER REPORTED VIA PHONE CALL THAT THEY HAD HYPERGLYCEMIA. BLOOD GLUCOSE LEVEL WAS 402 MG/DL. CUSTOMER STATED THAT BLOOD GLUCOSE NOT CAME DOWN AFTER BOLUS. CUSTOMER ALSO STATED THAT THE INSULIN PUMP WAS WORKING FINE. CUSTOMER HAD BEEN USING INSULIN PUMP SYSTEM WITHIN 48 HOURS OF REPORTED HIGH BLOOD GLUCOSE EVENT. CUSTOMER ALSO CONFIRMED ABOUT HAVING NO LEAKS ON THE SYSTEM. CUSTOMER ALSO EXPLAINED THAT THIS MORNING HIS BLOOD GLUCOSE WAS AROUND 50 MG/DL AND THEN SHOT UP TO AROUND 400 MG/DL. CUSTOMER TREATED THEIR HIGH BLOOD GLUCOSE WITH MANUAL INJECTIONS OR INSULIN PEN. CUSTOMER MENTION THAT THE INSULIN PUMP NOT GAVE HIM ALERT ON HIS HIGH BLOOD GLUCOSE. INSULIN PUMP WILL NOT BE RETURNED FOR ANALYSIS.

  Patient problems: Hyperglycemia; Hypoglycemia

  MAUDE report 10389319 ↗
• MalfunctionAug 10, 2020No Display/Image; No Display/Image

  INFORMATION RECEIVED BY MEDTRONIC INDICATED THAT THE INSULIN PUMP RECEIVED BLACK DISPLAY AFTER REPLACING BATTERY. CUSTOMER REMOVED BATTERY AND RECEIVED INSERT BATTERY ALARM. CUSTOMER CHECKED IF BATTERY CAP CONTACTS WERE DAMAGED OR MISSING. CUSTOMER CHECKED IF BATTERY COMPARTMENT AND SPRING WERE DAMAGED OR CORRODED. CUSTOMER INSERT BATTERY BUT DISPLAY DID NOT RETURN. NO HARM REQUIRING MEDICAL INTERVENTION WAS REPORTED. THE INSULIN PUMP WILL BE RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 10384355 ↗
• InjuryAug 10, 2020Adverse Event Without Identified Device or Use Problem; No Apparent Adverse Event; Adverse Event Without Identified Device or Use Problem; No Apparent Adverse Event

  THE CUSTOMER REPORTED VIA PHONE CALL THAT THEY WERE EXPERIENCING HIGH BLOOD GLUCOSE. BLOOD GLUCOSE LEVEL AT THE TIME OF THE INCIDENT WAS 566 MG/DL. CUSTOMER STATED THAT HER LAST BLOOD GLUCOSE WAS AT 88 MG/DL. CUSTOMER HAVE TAKEN INSULIN AND ITS NOT WORKING. CUSTOMER STATED THAT AUTO MODE FEATURE WAS NOT ACTIVE. THE INSULIN PUMP WILL NOT BE RETURNED FOR ANALYSIS.

  Patient problems: Hyperglycemia

  MAUDE report 10383689 ↗
• MalfunctionAug 10, 2020Obstruction of Flow; Obstruction of Flow

  INFORMATION RECEIVED BY MEDTRONIC INDICATED THAT THE INSULIN PUMP RECEIVED INSULIN FLOW BLOCK ALARM. THE CUSTOMER ALSO EXPERIENCED LOW BLOOD GLUCOSE LEVEL. THE CUSTOMER HAD CHANGED SET. THE CUSTOMER RECEIVED INSULIN FLOW BLOCK ALARM WHILE FILL TUBING. NO HARM REQUIRING MEDICAL INTERVENTION WAS REPORTED. THE INSULIN PUMP WILL BE RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 10383571 ↗
• MalfunctionAug 10, 2020Moisture or Humidity Problem; Power Problem; Moisture or Humidity Problem; Power Problem

  INFORMATION RECEIVED BY MEDTRONIC INDICATED THAT THE INSULIN PUMP HAD CRITICAL PUMP ERROR. CUSTOMER REPORTED THEY RECEIVED THE OPEN BOOK IMAGE ON THE INSULIN PUMP SCREEN AND EXPOSED TO MOISTURE. CUSTOMER STATED NO INSULIN PUMP ERROR DISPLAYED ON THE SCREEN BEFORE THE OPEN BOOK IMAGE. NO HARM REQUIRING MEDICAL INTERVENTION WAS REPORTED. THE INSULIN PUMP WILL BE RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 10383419 ↗
• InjuryAug 9, 2020Obstruction of Flow; Obstruction of Flow

  CUSTOMER REPORTED VIA PHONE CALL THAT THEY EXPERIENCED HIGH BLOOD GLUCOSE. THE CUSTOMER BLOOD GLUCOSE LEVEL WAS 574 MG/DL AT THE TIME OF INCIDENT. CUSTOMER REPORTED THAT THEY RECEIVED INSULIN FLOW BLOCKED ALARM. CUSTOMER REPORTED THAT THE EVENT WAS RESOLVED BY COMPLETE SET CHANGED. CUSTOMER TREATED WITH MANUAL INJECTION. THE INSULIN PUMP WILL NOT BE RETURNED FOR ANALYSIS.

  Patient problems: Hyperglycemia

  MAUDE report 10383300 ↗
• MalfunctionAug 7, 2020Mechanical Problem; Mechanical Problem

  INFORMATION RECEIVED BY MEDTRONIC INDICATED THAT THE INSULIN PUMP RECEIVED CRITICAL PUMP ERROR. OPEN BOOK IMAGE WAS SHOWING ON SCREEN. NO HARM REQUIRING MEDICAL INTERVENTION WAS REPORTED. THE INSULIN PUMP WILL BE RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 10378086 ↗
• InjuryAug 7, 2020Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  THE CUSTOMER REPORTED VIA PHONE CALL THAT THEY EXPERIENCE LOW BLOOD GLUCOSE. THE CUSTOMER¿S BLOOD GLUCOSE LEVEL WAS 40 MG/DL AND 61 MG/DL. CUSTOMER HAD USING INSULIN PUMP SYSTEM WITHIN 48 HOURS OF REPORTED HIGH BLOOD GLUCOSE EVENT. THE CUSTOMER TREATED THEMSELVES WITH FOOD AND JUICE AND DISCONNECTED FROM THE INSULIN PUMP. CUSTOMER WAS NEITHER IN EMERGENCY ROOM, NOR ADMITTED INTO HOSPITAL. THE INSULIN PUMP DID NOT ALARM ON LOW. THE CUSTOMER CHECKED THE AUDIO SETTINGS BUT STILL IT DID NOT ALARM. THE INSULIN PUMP WILL NOT BE RETURNED FOR ANALYSIS.

  Patient problems: Hypoglycemia

  MAUDE report 10377980 ↗

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-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-1740-2026 · Feb 13, 2026 · Open, Classified
  MiniMed 630G Insulin Pump (MMT-1714, MMT-1715, MMT-1754, MMT-1755)
• 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-1259-2025 · Jan 31, 2025 · Open, Classified
  MiniMed insulin pump, REF: 630G (MMT-1714, MMT-1715, MMT-1754, MMT-1755)
• 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-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-0955-2020 · Nov 21, 2019 · Open, Classified
  Medtronic MiniMed 630G System with SmartGuard, Ref/Model # MMT-1515, MMT-1715, MMT-1714, MMT-1754, and MMT-1755 *US and Canada Version Only

…and 6 more.