PlainRecalls

Medtronic MiniMed, Inc.

Compiled from official public sources by the publisher.

49 recalls on record · Latest: Jul 29, 2026

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Agency notice ledger

Federal filing book Medtronic MiniMed, Inc. MID-BOOK · SINGLE-AGENCY

#358 of 14,151 · 49 notices · 0.047% archive

  • BOOK 49 notices
  • RANK #358 of 14,151
  • SHARE 0.047% archive
  • AGENCY FDA Devices (49)
  • CAT medical devices
  • CATS 1 category
  • LATEST Jul 29, 2026
  • PHOTO Partell Specialty Pha…

Nearest notice-volume peer: Partell Specialty Pharmacy (0 notice gap)

Medtronic MiniMed, Inc. accounts for about 0.047% of the 104,423-notice archive on 49 distinct filings — a mid share signal beside absolute volume. FDA · CPSC · USDA FSIS · NHTSA notice stamps for this firm. Read with this firm → · Dominant category → · Similar-volume firm →

How Medtronic MiniMed, Inc. compares to 14,151 recalling firms

Medtronic MiniMed, Inc. ranks 358th of 14,151 tracked firms by distinct recall-event count. Archive size reflects filing volume, not inherent product danger.

Medtronic MiniMed, Inc. vs all firms by recall-notice count

Where this firm's archive sits among every tracked recalling manufacturer

49 358th of 14151 higher than 13,790 of 14,151 firms

Firms, banded by distinct federal recall-event inventory

Each bar is a band; taller bars hold more firms. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source FDA · CPSC · USDA FSIS · NHTSA federal recall filings · 2026-09-13

Medtronic MiniMed, Inc. in the notice-volume neighbourhood

Distinct federal recall events among this firm and nearest nationwide peers

notices

What this shows Medtronic MiniMed, Inc. holds about 0.047% of archive notices alongside 49 distinct filings.

Source FDA · CPSC · USDA FSIS · NHTSA filings aggregated by PlainRecalls As of September 2026
FDA Devices Moderate Jul 29, 2026

MiniMed Go App, Model: MMT-8600 (iOS), MMT-8601 (Android)
FDA Devices Moderate Jul 15, 2026

MiniMed 780G Insulin Pump, REF: MMT-1885, MMT-1886, MMT-1895, MMT-1896
FDA Devices Moderate Apr 8, 2026

MiniMed 720G Insulin Pump (MMT-1809, MMT-1810, MMT-1859, MMT-1860, MMT-1867)
FDA Devices Moderate Apr 8, 2026

Paradigm REAL-Time Insulin Pump (MMT-522, MMT-722)
FDA Devices Moderate Apr 8, 2026

Paradigm REAL-Time Veo Insulin Pump (MMT-554, MMT-754)
FDA Devices Moderate Apr 8, 2026

MiniMed 620G Insulin Pump (MMT-1750)
FDA Devices Moderate Apr 8, 2026

Paradigm Insulin Pump (MMT-712, MMT-715)
FDA Devices Moderate Apr 8, 2026

MiniMed 740G Insulin Pump (MMT-1811, MMT-1812, MMT-1861, MMT-1862)
FDA Devices Moderate Apr 8, 2026

Paradigm REAL-Time Revel Insulin Pump (MMT-523, MMT-723)
FDA Devices Moderate Apr 8, 2026

MiniMed 530G Insulin Pump (MMT-551, MMT-751)
FDA Devices Moderate Apr 8, 2026

MiniMed 780G Insulin Pump (MMT-1884, MMT-1885, MMT-1886, MMT-1894, MMT-1895, MMT-1896)
FDA Devices Moderate Apr 8, 2026

MiniMed 640G Insulin Pump (MMT-1711, MMT-1712, MMT-1751, MMT-1752)
FDA Devices Moderate Apr 8, 2026

MiniMed 630G Insulin Pump (MMT-1714, MMT-1715, MMT-1754, MMT-1755)
FDA Devices Moderate Apr 8, 2026

MiniMed 770G Insulin Pump (MMT-1880, MMT-1881, MMT-1882, MMT-1890, MMT-1891, MMT-1892)
FDA Devices Moderate Apr 8, 2026

MiniMed 700G Insulin Pump (MMT-1801, MMT-1805, MMT-1850, MMT-1851)
FDA Devices Moderate Apr 8, 2026

MiniMed 670G Insulin Pump (MMT-1760, MMT-1761, MMT-1762, MMT-1780, MMT-1781, MMT-1782)
FDA Devices Moderate Apr 1, 2026

MiniMed" 780G - MMT-1884 MiniMed" 780G - MMT-1886 With Software 6.60 and 6.61
FDA Devices Moderate Feb 11, 2026

MiniMed 780G Insulin Pump Catalog Numbers: MMT-1884 MMT-1886 With Software Version 6.60 The MiniMed 780G insulin pump is indicated for use by patients age 7-80 years with Type 1 diabetes, whose total daily dose of insulin is 8 units per day or more. The MiniMed 780G system is intended for continuous delivery of basal insulin at selectable rates, and the administration of insulin boluses at selectable amounts for the management of type 1 diabetes mellitus in persons seven years of age and o
FDA Devices Moderate Dec 24, 2025

InPen App, Model/CFN Number: MMT-8061 (Android Users)
FDA Devices Moderate Dec 3, 2025

CareLink Clinic, REF: MMT-7350
FDA Devices Moderate Oct 8, 2025

Medtronic, Simplera Sensor, REF: MMT-5100JD1
FDA Devices Moderate Sep 10, 2025

InPen App, CFN: MMT-8060 (iOS Users) and MMT-8061 (Android Users)
FDA Devices Moderate Apr 30, 2025

InPen smart insulin pen, REF: MMT-105NNBLNA, MMT-105NNGYNA, MMT-105NNPKNA, MMT-105ELBLNA, MMT-105ELGYNA, MMT105ELPKNA
FDA Devices Moderate Mar 12, 2025

MiniMed insulin pump, REF: 770G (MMT-1880, MMT-1881, MMT-1882, MMT-1890, MMT-1891, MMT-1892)
FDA Devices Moderate Mar 12, 2025

MiniMed insulin pump, REF: 630G (MMT-1714, MMT-1715, MMT-1754, MMT-1755)
FDA Devices Moderate Mar 12, 2025

MiniMed insulin pump, REF: 720G (MMT-1809, MMT-1810, MMT-1859, MMT-1860, MMT-1867)
FDA Devices Moderate Mar 12, 2025

Paradigm REF: MMT-712 and MMT-715
FDA Devices Moderate Mar 12, 2025

MiniMed insulin pump, REF: 620G (MMT-1750)
FDA Devices Moderate Mar 12, 2025

Paradigm insulin pump, REF: MMT-754
FDA Devices Moderate Mar 12, 2025

MiniMed insulin pump, REF: 640G (MMT-1711, MMT-1712, MMT-1751, MMT-1752)
FDA Devices Moderate Mar 12, 2025

Paradigm insulin pump, REF: MMT-522, MMT-523, MMT-551, MMT-722, MMT-723, MMT-751
FDA Devices Moderate Mar 12, 2025

MiniMed insulin pump, REF: 670G (MMT-1760, MMT-1761, MMT-1762, MMT-1780, MMT-1781, MMT-1782)
FDA Devices Moderate Mar 12, 2025

MiniMed insulin pump, REF: 740G (MMT-1811, MMT-1812, MMT-1861, MMT-1862)
FDA Devices Moderate Mar 12, 2025

MiniMed insulin pump, REF: 700G (MMT-1801, MMT-1805, MMT-1850, MMT-1851)
FDA Devices Moderate Mar 12, 2025

MiniMed insulin pump, REF: 780G (MMT-1884, MMT-1885, MMT-1886, MMT-1894, MMT-1895, MMT-1896)
FDA Devices Critical Oct 9, 2024

MiniMed 620G Insulin Pump, REF: MMT-1510, MMT-1710, MMT-1750; MiniMed 630G Insulin Pump, REF: MMT-1515, MMT-1714, MMT-1715, MMT-1754, MMT-1755; MiniMed 640G Insulin Pump, REF: MMT-1511, MMT-1711, MMT-1512, MMT-1712, MMT-1751, MMT-1752; MiniMed 720G Insulin Pump, REF: MMT-1809, MMT-1810, MMT-1817, MMT-1818, MMT-1859, MMT-1860, MMT-1867, MMT-1868 MiniMed 740G Insulin Pump, REF: MMT-1811, MMT-1812, MMT-1861, MMT-1862
FDA Devices Critical Oct 9, 2024

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, REF: MMT-1880, MMT-1881, MMT-1882, MMT-1890, MMT-1891, MMT-1892; MiniMed 780G, REF: MMT-1884, MMT-1885, MMT-1886, MMT-1894, MMT-1895, MMT-1896
FDA Devices Critical Oct 9, 2024

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
FDA Devices Moderate Feb 14, 2024

Guardian 4 Glucose Sensor, REF: MMT-7040A, MMT-7040C1, MMT-7040C2, MMT-7040C3, MMT-7040D1, MMT-7040D2, MMT-7040MA, MMT-7040QC1, MMT-7040QC2, MMT-7040QC3
FDA Devices Moderate Apr 27, 2016

CareLink iPro2 Reports, Model No. MMT-7340 is software intended to retrospectively calibrates sensor data and provides reports of continuous glucose information
FDA Devices Moderate Dec 23, 2015

MiniMed 640G, 3.0mL mmol/L, 3.0mL mg/dL, Model No. MMT-1711 and MMT-1712 The MiniMed 620G and MiniMed 640G insulin pump systems are indicated for the continuous delivery of insulin, at set and variable rates, for the management of diabetes mellitus in persons requiring insulin. In addition, the pump system is indicated for continuous monitoring of glucose levels in the fluid under the skin, and possible low and high blood glucose episodes.
FDA Devices Moderate Dec 23, 2015

MiniMed 620G, 3.0mL mg/dL, Model No. MMT-1710 The MiniMed 620G and MiniMed 640G insulin pump systems are indicated for the continuous delivery of insulin, at set and variable rates, for the management of diabetes mellitus in persons requiring insulin. In addition, the pump system is indicated for continuous monitoring of glucose levels in the fluid under the skin, and possible low and high blood glucose episodes.
FDA Devices Moderate Sep 2, 2015

Guardian Real-Time Monitor, Model No. CSS7100. Indicated for continuous or periodic monitoring of glucose levels in the fluid under the skin, in adults (18 years and older) with diabetes mellitus, for the purpose of improving diabetes management.
FDA Devices Moderate Aug 5, 2015

MiniMed NGP 640G 1.8ml (mmol/L), Model No. MMT-1511; NGP 640G 1.8ml (mg/dL), Model No. 1512; NGP 640G PLGM 3ml (mmol/L), Model No. MMT-1711; NGP 640G PLGM 3ml (mg/dL), Model No. MMT-1712.
FDA Devices Low Mar 11, 2015

CareLink Pro Medtronic CareLink Pro MMT-7335 is a personal computer software application designed to enhance Health Care Provider management of diabetic patients using Medtronic insulin pumps and blood glucose meters. MMT-7335 is intended for use by Health Care Providers/Physicians as a therapy management accessory to: - read and store history and settings data supported insulin pump models and supported blood glucose meters - read and report user-programmable settings on supported pump mode
FDA Devices Moderate Dec 17, 2014

Medtronic MiniMed Silhouette and/or MiniMed Sure-T Infusion Sets; Paradigm Silhouette infusion sets: MMT-368, MMT-368600, MMT-371, MMT-373, MMT-377, MMT-377600, MMT378, MMT-378600, MMT-38 1, MMT-381 600, MMT-382, MMT-382600, MMT-383, MMT-383600, MMT384, & MMT384600. Sure-T infusion sets MMT-862, MMT-863, MMT-864, MMT-865, MMT-866, MMT-873, MMT-874, MMTMMT-875, MMT-876, MMT-884, & MMT-886. MiniMed Duo sensor/infusion sets: MMT-5001A23, MMT-5001A43, MMT-5001B23, MMT-5001B43, MMT-5011A23, MMT-5011A
FDA Devices Moderate Sep 3, 2014

Medtronic MiniMed Paradigm Insulin Infusion Pumps, Paradigm models: MMT-511, MMT-512, MMT-712, MMT-712E, MMT-515, MMT-715, MMT-522, MMT-522K, MMT-722, MMT-722K, MMT-523, MMT-523K, MMT-723, MMT-723K, MMT-554, and MMT-754. MiniMed 530G: MMT-551, and MMT-751 Paradigm insulin infusion pumps are intended for use to deliver basal and bolus insulin to persons with diabetes.
FDA Devices Moderate Aug 20, 2014

Medtronic MiniMed Guardian Monitor, Model No. CSS7100, CSS7100K Product Usage: The Medtronic MiniMed model CSS7100 and CSS7100K Guardian REAL-Time monitors are used in combination with the Minilink transmitter and Sof-sensor glucose sensor for continuous monitoring of subcutaneous glucose concentration. The information provided by these devices is intended for use in identifying potential episodes of high or low blood glucose. The information provided is not intended to be used directly for

FDA Devices Moderate Aug 20, 2014

Medtronic MiniMed Implantable Insulin Pump, Model No. MMT-2007D

Medtronic MiniMed, Inc. holds a measurable archive slice

Drug and device firms outside this manufacturer and state, matched by notice volume and category footprint.

Frequently Asked Questions

How many federal recall notices name Medtronic MiniMed, Inc.? ▼
PlainRecalls indexes 49 distinct federal recall events naming Medtronic MiniMed, Inc., aggregated from FDA, CPSC, USDA FSIS, and NHTSA filings (archive as of September 2026). That count is an issuance inventory, not a hazard score.
Where does Medtronic MiniMed, Inc. sit among other recalling firms? ▼
Medtronic MiniMed, Inc. ranks #358 of 14,151 by distinct recall-event count among 14,151 firms in this archive (97th percentile of firms with fewer notices). Rank tracks filing frequency, not product danger.
Which agency issues most of Medtronic MiniMed, Inc.'s notices? ▼
FDA Devices accounts for 49 of this firm's 49 indexed notices.
What product category dominates Medtronic MiniMed, Inc.'s filing book? ▼
Filings for Medtronic MiniMed, Inc. span 1 product category, led by medical devices. Browse that category archive for peer firms and related notices.
Is a higher notice count more dangerous? ▼
No. Archive size reflects how often federal agencies publish recalls naming the firm — reporting volume, coverage, and product range all move the number. Always verify the individual notice with the issuing agency before acting on a specific product.
Medtronic MiniMed, Inc.: 49 federal recall notices aggregated from FDA, CPSC, USDA FSIS, and NHTSA filings (lead agency FDA Devices). Verify individual notices with FDA directly before acting on a specific recall.

Firm-level totals aggregate distinct federal recall events naming Medtronic MiniMed, Inc.; individual notices remain authoritative on each linked recall page.

Methodology · Corrections · FDA · CPSC · USDA FSIS · NHTSA · Archive as of September 2026