Medtronic EVX 60 Series - Medical Devices
Medtronic EVX 60 Series: Advanced medical devices for healthcare applications. Explore the latest EVX 60 Series products and solutions.
Lower-risk recall
There is a potential for delayed time to high-voltage (HV) therapy should a rare sequence of events occur.
Contact the company
What happened, in plain English
The Medtronic EVX 60 Series is a range of medical devices designed for healthcare applications. This series includes various models such as EVX605584, EVX605584S, EVX605585, etc. These devices are used in medical settings to provide critical healthcare services. Read more at govinfonow.com/recall/50935-medtronic-evx-60-series-medical-devices.
Source Summary by GovInfoNow · govinfonow.com/recall/50935-medtronic-evx-60-series-medical-devices · Updated August 10, 2026 · FDA enforcement record: FDA #Z-0726-2026
Cite this page
“Medtronic EVX 60 Series - Medical Devices.” GovInfoNow, updated August 10, 2026. https://govinfonow.com/recall/50935-medtronic-evx-60-series-medical-devices. Based on FDA recall #Z-0726-2026 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0726-2026%22&limit=1).
Why it’s dangerous
The EVX 60 Series is a medical device series with low risk of harm when used correctly. However, improper use or malfunction could lead to adverse effects.
Who’s affected
Healthcare professionals, medical device users, and patients
How to tell if you have this one
Ensure proper installation, regular maintenance, and adherence to manufacturer guidelines for safe operation.
- Brand
Medtronic- Category
Medical device
What to do — step by step
What to do if the device is malfunctioning
Contact Medtronic customer support immediately for assistance.
How to ensure safe usage
Follow the manufacturer's instructions for installation, operation, and maintenance.
Where it went and when
Where it was distributed
Distributed nationwide, and outside the U.S.
FDA distribution: “Worldwide - US Nationwide distribution.” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide, and outside the U.S.
Recall timeline
FDA published this recall 42 days after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
Dates from the agency record only; steps without a date are left out.
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Where this comes from
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
- Official source: FDA Recall #Z-0726-2026 (October 29, 2025) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0726-2026 to see it in context.
- Plain-language summary written by qwen3:4b on August 10, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.