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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Critical RiskFDA Device
Medical Devices/Home Healthcare

Medtronic MiniMed Insulin Pumps Recalled for Battery and Power Loss Risks

Agency Publication Date: October 3, 2024
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Summary

Medtronic MiniMed, Inc. has recalled approximately 785,513 insulin pumps, including several models in the 600 and 700 series, because they may experience sudden power loss or shortened battery life if they have been dropped, bumped, or otherwise physically impacted. This physical damage can shorten the overall life of the battery and significantly reduce the lead time between a "low battery" alarm and when the device shuts off entirely. In some cases, the buffer time can drop from the expected 10 hours down to just 2.5 hours or less. Replacing the battery does not resolve the underlying electrical damage. The recall affects models 620G, 630G, 640G, 670G, 700G, 720G, 740G, 770G, and 780G.

Risk

If the insulin pump powers down unexpectedly without adequate warning, it can lead to an interruption in insulin delivery. This interruption may result in dangerously high blood sugar (hyperglycemia) or diabetic ketoacidosis (DKA), which is a serious medical emergency. Patient reports indicate that some devices shut off almost immediately after the low battery alert.

What You Should Do

  1. This recall involves Medtronic MiniMed 600 and 700 series insulin pumps, including models 620G, 630G, 640G, 670G, 700G, 720G, 740G, 770G, and 780G.
  2. To identify if your device is affected, look for the model (REF) number on the pump label or find it within the pump settings menu. See the Affected Products section below for the full list of affected codes.
  3. Stop using the product and contact your healthcare provider or the manufacturer if your pump experiences rapid battery depletion, repeated low battery alarms, or physical damage from being dropped.
  4. Contact Medtronic MiniMed, Inc. or your distributor directly to arrange for a device return, replacement, or correction instructions.
  5. Call the FDA Consumer Complaint hotline at 1-888-463-6332 for additional questions regarding this recall.

Your Remedy Options

You have 2 options:

๐Ÿ’ฐOption 1: Full Refund
How to: Contact your healthcare provider, or return the product to the place of purchase for a refund or replacement
๐Ÿ—‘๏ธOption 2: Dispose of Product
How to: Stop using and throw the product away.

Affected Products

Product: MiniMed 630G and 700G Insulin Pumps (Recall Z-0001-2025)
Model / REF:
MMT-1515
MMT-1714
MMT-1715
MMT-1754
MMT-1755
MMT-1800
MMT-1801
MMT-1805
MMT-1850
MMT-1851
Serial Numbers:
All serial numbers
GTIN:
00643169782396
00763000253059
00643169873841
00763000190446
00643169752726
643169873834
00763000317591
00763000316655
763000367053
763000316655
76300031665503
763000190439
763000316631
763000166519
763000072520
76300031665501
763000256807
763000090197
643169656840
763000316686
00643169656840
00763000090197
00763000190439
00763000316631
643169752726
643169873841
763000190446
763000101527
763000317591
763000367091
763000179632
763000317621
643169878648
763000157043
76300031759103
76300031759101
76300031762103
76300031762101
00763000101527
00763000531157
00763000561680
00763000552541
00763000854737
00763000541323

Units affected: 24,595

Product: MiniMed 620G, 630G, 640G, 720G, and 740G Insulin Pumps (Recall Z-0002-2025)
Model / REF:
MMT-1510
MMT-1710
MMT-1750
MMT-1515
MMT-1714
MMT-1715
MMT-1754
MMT-1755
MMT-1511
MMT-1711
MMT-1512
MMT-1712
MMT-1751
MMT-1752
MMT-1809
MMT-1810
MMT-1817
MMT-1818
MMT-1859
MMT-1860
MMT-1867
MMT-1868
MMT-1811
MMT-1812
MMT-1861
MMT-1862
Serial Numbers:
All serial numbers
GTIN (657):
00643169568419
00763000253189
00763000375461
00643169721319
00643169559745
763000253189
00763000253059
00763000074845
00643169782396
763000253059
643169782396
00763000316631
763000190439
763000316631
00763000253066
00643169976344
00763000315719
00763000381912
763000253066
643169752726
643169873841
763000190446
763000101527
763000317591
00763000317591
763000367091
763000179632
763000317621
643169878648
763000157043
76300031759103
00643169752726
76300031759101
76300031762103
76300031762101
00763000101527
00763000190446
00643169662568
00763000317119
00763000317089
00763000404550
00763000367039
00763000317102
00643169662544
00643169739468
00643169554931
00763000192136
00763000068998
00763000198596
00643169662575

Units affected: 234,360

Product: MiniMed 670G, 770G, and 780G Insulin Pumps (Recall Z-0003-2025)
Model / 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
MMT-1880
MMT-1881
MMT-1882
MMT-1890
MMT-1891
MMT-1892
MMT-1884
MMT-1885
MMT-1886
MMT-1894
MMT-1895
MMT-1896
Serial Numbers:
All serial numbers
GTIN (251):
00763000190453
00643169946057
00763000365882
00763000096984
00763000283445
763000283513
763000283506
763000283520
76300028351303
763000393786
763000166526
76300028351301
643169939202
763000190460
763000090203
763000256821
643169939219
763000072537
763000365912
00763000090203
00763000190460
00763000283520
00763000393786
00763000187415
00763000283568
00763000283544
00763000404536
00763000283551
00763000283537
00763000365899
00763000371937
00763000225575
00763000225582
00763000235765
00763000187378
00763000140601
763000240707
763000187378
763000140601
763000283544
00763000187422
00763000235772
00763000283599
00763000264727
00763000404543
00763000283582
00763000371944
00763000365905
00763000283575
00643169957640

Units affected: 526,558

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 95121
Status: Active
Manufacturer: Medtronic MiniMed, Inc.
Sold By: Medtronic MiniMed, Inc.; Authorized Medical Device Distributors
Manufactured In: United States
Units Affected: 3 products (24,595; 234,360; 526,558)
Distributed To: Connecticut, Michigan, Pennsylvania, Washington, Iowa, New York, North Dakota, Arizona, Texas, Ohio, North Carolina, Alabama, Minnesota, Indiana, New Jersey, Kentucky, Utah, California, Florida, Virginia, Mississippi, New Mexico, Nevada, Tennessee, Georgia, Massachusetts, New Hampshire, Oklahoma, Vermont, Illinois, Maine, South Carolina, Louisiana, Wyoming, Rhode Island, South Dakota, Kansas, Wisconsin, Maryland, Colorado, Delaware, Arkansas, Alaska, Idaho, Missouri, Nebraska, West Virginia, Montana, Oregon, District of Columbia, Hawaii, U.S. Virgin Islands, Puerto Rico

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

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This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES ยท Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.