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Recall Observatory FDA recall evidence

Derived label

Device software or design

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

reason.device_software_design

v1.0.0

Assignment summary

Mode key
device_software_design
Evidence excerpt
cybersecurity vulnerability
Rule explanation
Device recall wording explicitly identifies a software, firmware, programming, cybersecurity, or design defect and its failure or consequence.
Firm
Medtronic MiniMed

Field note

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