Is MiniMed Insulin Pump, model # MMT-508 recalled?

Medium RiskFDA Device

Medtronic MiniMed: The action is being initiated due to potential cybersecurity vulnerabilities related to a series of insulin pumps that are designed to communicate using a wireless radio frequency (RF). An unauthorized person could potentially connect wirelessly to a nearby insulin pump to change settings and control insulin delivery.

Agency Publication Date: March 26, 2020

Affected Products

Product: MiniMed Insulin Pump, model # MMT-508

All Software Versions

Product: MiniMed Paradigm Model 511 Insulin Pump

All Software Versions

Product: MiniMed Paradigm 512 Insulin pump

All Software Versions

Product: MiniMed Paradigm Insulin pump, model number MMT-712

All software Versions

Product: Medtronic MiniMed Paradigm Insulin pump, model number MMT-712E

All software Versions Available outside the US only.

Product: Medtronic MiniMed Paradigm Insulin pump, model numbers MMT 515 and MMT-715

All software versions

Product: Medtronic MiniMed Paradigm Insulin pump, model number MMT-522

All software versions

Product: Medtronic MiniMed Paradigm Insulin pump, model number MMT-722

All software Versions

Product: Medtronic MiniMed Paradigm Insulin pump, model number MMT-522K

All Software Versions

Product: Medtronic MiniMed Paradigm Insulin pump, model number MMT-722K

All Software versions

Product: Medtronic MiniMed Paradigm Insulin pump, model number MMT-523

All software versions 2.4A or lower

Product: Medtronic MiniMed Paradigm Insulin pump, model number MMT-523K

All software versions 2.4A or lower

Product: Medtronic MiniMed Paradigm Insulin pump, model number MMT-723K

All software versions 2.4A or lower

Product: Medtronic MiniMed Paradigm Insulin pump, model number MMT-723

All software versions 2.4A or lower

Product: Medtronic MiniMed Paradigm Veo Insulin pump, model numbers MMT-554 and MMT-754

All software versions 2.6A or lower. Available outside the US only.

Product: Medtronic MiniMed Paradigm Veo Insulin pump, model numbers MMT-554CM and MMT-754CM

All software versions 2.7A or lower. Available outside the US only.

Additional Information

Agency: Food and Drug Administration (FDA)

Event ID: 83433

Status: Active

Manufacturer: Medtronic MiniMed

Manufactured In: United States

Units Affected: 16 products (64,174 units; 30,479; 34,777; 74,496; 36,143; 73,028; 88,243; 225,498; 38; 17; 23,221; 27; 10; 72,850; 68,598; 2,322)

Agency Last Updated: February 28, 2023

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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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 · 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.

Affected Products

Product: MiniMed Insulin Pump, model # MMT-508

All Software Versions

Product: MiniMed Paradigm Model 511 Insulin Pump

All Software Versions

Product: MiniMed Paradigm 512 Insulin pump

All Software Versions

Product: MiniMed Paradigm Insulin pump, model number MMT-712

All software Versions

Product: Medtronic MiniMed Paradigm Insulin pump, model number MMT-712E

All software Versions Available outside the US only.

Product: Medtronic MiniMed Paradigm Insulin pump, model numbers MMT 515 and MMT-715

All software versions

Product: Medtronic MiniMed Paradigm Insulin pump, model number MMT-522

All software versions

Product: Medtronic MiniMed Paradigm Insulin pump, model number MMT-722

All software Versions

Product: Medtronic MiniMed Paradigm Insulin pump, model number MMT-522K

All Software Versions

Product: Medtronic MiniMed Paradigm Insulin pump, model number MMT-722K

All Software versions

Product: Medtronic MiniMed Paradigm Insulin pump, model number MMT-523

All software versions 2.4A or lower

Product: Medtronic MiniMed Paradigm Insulin pump, model number MMT-523K

All software versions 2.4A or lower

Product: Medtronic MiniMed Paradigm Insulin pump, model number MMT-723K

All software versions 2.4A or lower

Product: Medtronic MiniMed Paradigm Insulin pump, model number MMT-723

All software versions 2.4A or lower

Product: Medtronic MiniMed Paradigm Veo Insulin pump, model numbers MMT-554 and MMT-754

All software versions 2.6A or lower. Available outside the US only.

Product: Medtronic MiniMed Paradigm Veo Insulin pump, model numbers MMT-554CM and MMT-754CM

All software versions 2.7A or lower. Available outside the US only.

Additional Information

Agency: Food and Drug Administration (FDA)

Event ID: 83433

Status: Active

Manufacturer: Medtronic MiniMed

Manufactured In: United States

Units Affected: 16 products (64,174 units; 30,479; 34,777; 74,496; 36,143; 73,028; 88,243; 225,498; 38; 17; 23,221; 27; 10; 72,850; 68,598; 2,322)

Agency Last Updated: February 28, 2023