MiniMed® 670G MMT-1780KL (UDI 00763000256821)Recalls & reported problems

Medtronic Minimed, Inc. · PUMP MMT-1780KL 670G V4.11 JBL MG · Class 3

All models of MiniMed 670G (23)

Data updated Oct 16, 2026 from official FDA records · Editorial policy

2 open recalls name this device. See the recall details and contact the manufacturer or your healthcare provider.

Quick summary

This MiniMed 670G insulin pump has 374 reports, with no deaths and 93 injuries. Many describe power problems, cracked or broken parts, and blank screens, and some mention high or low blood sugar. There are 2 recalls, both still open: a 2026 one over insulin over- or under-delivery when the pump is raised or lowered, and a 2024 one over pumps that were dropped or bumped and may lose battery life.

AI-generated from the FDA records on this page and checked automatically against the numbers below. Read the details before relying on it.

Adverse event reports: 374
Deaths reported: 0
Injuries reported: 93
Recalls naming it: 2

Summary

The FDA's MAUDE database contains 374 adverse event reports that list this exact device (DI 00763000256821), received between Sep 5, 2019 and Jul 27, 2022 — classified as 93 injuries, 281 malfunctions.

The most frequently reported specific device problem is “Patient Device Interaction Problem” (131 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 16, 2026.

Recalls naming this device

Feb 13, 2026Open, 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 ↗
Jul 31, 2024Open, 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

Device problems

Patient Device Interaction Problem131
Adverse Event Without Identified Device or Use Problem85
No Apparent Adverse Event65
Power Problem50
Break45
No Display/Image28
Mechanical Problem24
Connection Problem19

Patient problems

No Consequences Or Impact To Patient202
Hyperglycemia80
No Clinical Signs, Symptoms or Conditions60
Hypoglycemia34
Elevated Ketones/ Diabetic Ketoacidosis9
Nausea6
Abdominal Pain4
Vomiting4

Recent adverse event reports

The 25 most recent of 374 reports, in the reporter's own words as published by the FDA.

MalfunctionJul 27, 2022Break; Break
INFORMATION RECEIVED BY MEDTRONIC INDICATED THAT INSULIN PUMP HAD CRACKED RETAINER RING AND THE RESERVOIR WAS ABLE LOCK IN PLACE. NO HARM REQUIRING MEDICAL INTERVENTION WAS REPORTED. THE CUSTOMER WILL DISCONTINUE TO USE THE DEVICE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 15113648 ↗
MalfunctionJul 8, 2022Break
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 14954573 ↗
MalfunctionJul 8, 2022Break
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 14954333 ↗
MalfunctionJul 8, 2022Break
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 14953770 ↗
MalfunctionJul 8, 2022Break
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 14952944 ↗
MalfunctionJul 4, 2022No Display/Image; Electrical /Electronic Property Problem; Device Markings/Labelling Problem
MEDTRONIC RECEIVED INFORMATION THAT BLANK DISPLAY, LABELING ANOMALY, PUMP ERROR 23 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 14906174 ↗
MalfunctionJul 4, 2022Power Problem; Intermittent Loss of Power
MEDTRONIC RECEIVED INFORMATION THAT PUMP ERROR 82, UNEXPECTED BATTERY POWER LOSS 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 14905788 ↗
MalfunctionJul 4, 2022Electrical /Electronic Property Problem
MEDTRONIC RECEIVED INFORMATION THAT PUMP ERROR 23 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 14905082 ↗
MalfunctionJul 4, 2022Break
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 14904577 ↗
MalfunctionJul 4, 2022Circuit Failure; Electrical /Electronic Property Problem; Communication or Transmission Problem; Intermittent Communication Failure
MEDTRONIC RECEIVED INFORMATION THAT PUMP ERROR 24, PUMP ERROR 3, PUMP ERROR 81, PUMP ERROR 23 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 14904472 ↗
MalfunctionJun 29, 2022Break
MEDTRONIC RECEIVED INFORMATION THAT DAMAGE (PHYSICAL OR COSMETIC) OCCURRED. THERE WAS AN ALLEGATION OF HYPERGLYCEMIA AS A RESULT OF THIS EVENT.
Patient problems: Hyperglycemia
MAUDE report 14865285 ↗
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 14823872 ↗
MalfunctionJun 25, 2022Break
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 14816170 ↗
MalfunctionJun 25, 2022Break
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 14816080 ↗
MalfunctionJun 25, 2022Break
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 14813855 ↗
MalfunctionJun 24, 2022No Display/Image; Material Integrity Problem
MEDTRONIC RECEIVED INFORMATION THAT BATTERY CAP CRACKED/DAMAGED, BLANK DISPLAY 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 14796444 ↗
MalfunctionJun 24, 2022Material Integrity 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 14796376 ↗
MalfunctionJun 23, 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 14795673 ↗
MalfunctionJun 23, 2022Material Integrity 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 14795565 ↗
MalfunctionJun 23, 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 14795227 ↗
MalfunctionJun 23, 2022Break
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 14785741 ↗
MalfunctionJun 23, 2022Break
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 14785079 ↗
MalfunctionJun 23, 2022Break
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 14784787 ↗
MalfunctionJun 22, 2022Break
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 14782382 ↗
MalfunctionJun 22, 2022Break
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 14781654 ↗

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-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-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-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-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.

Device details

UDI-DI	`00763000256821`
Brand	MiniMed® 670G
Model	MMT-1780KL
Company	Medtronic Minimed, Inc.
Product code	OZP · Automated insulin dosing device system, single hormonal control
Class	Class 3
FDA submission	P160017
Implant	No
Rx / OTC	Prescription
Single use	No
Sterile	No
MRI safety	MR Unsafe
Status	In Commercial Distribution
Record updated	Apr 3, 2023

Device type (GMDN): Ambulatory insulin infusion pump, electronic, software-dosing, binary algorithm

A portable electronic device designed to provide continuous or intermittent subcutaneous delivery of insulin to a patient with diabetes mellitus, incorporating software to receive glucose status data from a monitor/transmitter and to determine the delivery of insulin based on pre-set thresholds using a dichotomous or binary algorithm. It may be badge-like, designed to adhere to skin or clothing or worn in a case attached to the belt or carried in a pocket and includes a reservoir, a pumping mechanism, and an infusion-rate controller. It may also allow additional manual administration/infusion and functionality to send data to a remote reporting system.

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Sources and updates

Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026 · each recall links to the FDA recall notice
Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.

How reports and recalls are matched · Editorial policy · Report an error on this page