Reported Nov 16, 2022 · Ongoing

Insulin Pump/Model: MiniMed 630G/ MMT-1715, MMT-1755, MMT-1754; MiniMed 670G/ MMT-1780, MMT-1781, MMT-1782, MMT-1760,…

Medtronic MiniMed

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Medtronic MiniMed · 18000 Devonshire St · Northridge, CA · 91325-1219

Is this the product you have?

  • 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
Lot codes and dates

12 of 12 products

Products covered by this recall
#BarcodesProduct as published
164300000000076300007252064316987383400643169656840MMT-1715/643000000000, 763000072520, 643169873834, 00643169656840
264316975272664316987384164316987864876300017963200643169752726MMT-1755/643169752726, 643169873841, 643169878648, 763000179632, 00643169752726
3643169976344MMT-1754/643169976344
464316994970664316993920276300007253764300000000000643169939219MMT-1780/643169949706, 643169939202, 763000072537, 643000000000, 00643169939219
5763000187415763000283568007630001406010076300022557500763000235765007630001874150076300028355100763000240707MMT-1781/763000187415, 763000283568, 00763000140601, 00763000225575, 00763000235765, 00763000187415, 00763000283551, 00763000240707
6763000187422763000283599007630001406180076300022561200763000235772007630001874220064316995764000763000283582MMT-1782/763000187422, 763000283599, 00763000140618, 00763000225612, 00763000235772, 00763000187422, 00643169957640, 00763000283582
764316994604076300027842776300017964964316994605776300036708400643169946057MMT-1760/643169946040, 763000278427, 763000179649, 643169946057, 763000367084, 00643169946057
80076300036765700763000165413MMT-1761/00763000367657, 00763000165413
90076300023940400763000203313007630002164810076300018740800763000165475MMT-1762/00763000239404, 00763000203313, 00763000216481, 00763000187408, 00763000165475
10MMT-1740/Investigational
110076300030355600763000408916MMT-1741/00763000303556, 00763000408916
1200763000250232MMT-1742/00763000250232
Amount recalled
399651

This recall covers 2 products

The agency filed one notice per product. You are reading one of them; the other one is below.

Where it was sold

Why it was recalled

Medtronic identified a cybersecurity vulnerability in the MiniMed 600 series Insulin Pump Systems associated with the communication protocol that could allow unauthorized access to the pump system. This unauthorized access could be used to deliver too much or too little insulin through delivery of an unintended insulin bolus or because insulin delivery is slowed or stopped, which could lead to hypoglycemia or hyperglycemia. The Remote Bolus feature on insulin pumps should be turned off to prevent the unauthorized access.

This product could cause temporary or reversible health problems — stop using it.

Want the full recall guide?

The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.

Free recall alerts

Get alerted about new Medtronic MiniMed recalls

One email when a matching recall is published. No account, no cost, unsubscribe in one click.

Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Data as of Sep 19, 6:17 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.