Medtronic MiniMed Paradigm Veo Insulin Pumps Recalled for Cybersecurity Vulnerabilities
Medtronic MiniMed is recalling 2,322 Paradigm Veo insulin pumps due to cybersecurity vulnerabilities that could allow unauthorized wireless control of insulin delivery.
What this means for you
Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.
Our severity reasoning: The recall involves a high-risk medical device (insulin pump) where unauthorized control could lead to serious harm, but the source text does not report any actual injuries, illnesses, or deaths, fitting the 'High' severity criteria for risk-of-harm products without reported injury.
Plain-English summary
Medtronic MiniMed is recalling 2,322 units of the MiniMed Paradigm Veo Insulin pump, specifically model numbers MMT-554CM and MMT-754CM. The recall covers all software versions 2.7A or lower. These devices were distributed nationwide in the United States, including Puerto Rico.
The recall is being initiated due to potential cybersecurity vulnerabilities related to the pumps' wireless radio frequency (RF) communication capabilities. The source text states that an unauthorized person could potentially connect wirelessly to a nearby insulin pump to change settings and control insulin delivery.
Consumers who have these specific model numbers and software versions should contact Medtronic MiniMed for instructions on how to proceed. The source text does not provide specific contact details or a timeline for the recall resolution.
The recalled product
- Product
- Medtronic MiniMed Paradigm Veo Insulin pump, model numbers MMT-554CM and MMT-754CM
- Manufacturer
- Medtronic MiniMed
- Category
- Medical Device — Insulin Pump
- Affected units
- 2,322
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (1)
- All software versions 2.7A or lower. Available outside the US only.
Distribution
Part of a larger recall action
This product is one of 16 recalled by Medtronic MiniMed under a single FDA (Devices) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
See all 16 products in this recall →Related recalls
Same manufacturer · Medtronic MiniMed
See all →- HighGuardian Glucose Monitoring App May Automatically Log Out and Block Data Upload
FDA (Devices) · 2023-01-11
- HighMedtronic MiniMed Insulin Pumps Recalled for Cybersecurity Vulnerability
FDA (Devices) · 2022-11-16
- HighInsulin Pump Cybersecurity Vulnerability Allows Unauthorized Remote Access
FDA (Devices) · 2022-11-16
- HighMiniMed 630G Insulin Pump Recalled for Battery Cap Deterioration
FDA (Devices) · 2022-07-20
- HighMiniMed 620G insulin pump battery cap deterioration may cause power loss
FDA (Devices) · 2022-07-20
Same hazard · cybersecurity vulnerability
See all →- HighGE Healthcare Portrait Core Services Software Recall Due to Software Vulnerability
FDA (Devices) · 2026-08-12
- ModerateVersius Surgical System Console affected by cybersecurity vulnerability
FDA (Devices) · 2026-07-15
- HighWHILL Model C2 Powered Wheelchair Recalled for Bluetooth Security Vulnerability
FDA (Devices) · 2026-05-06
- HighGE Centricity Viewer 7.0 may expose login credentials on workstations
FDA (Devices) · 2026-03-25
- HighGE Centricity Viewer 5.0 may expose login credentials on workstations
FDA (Devices) · 2026-03-25