EasyOne Pro Respiratory Device Recall: CO/CO2 Sensor Cable Shielding Issue
NDDd Medical Technologies recalls EasyOne Pro Model 3000-1 respiratory devices due to potential CO/CO2 sensor interference from electromagnetic signals. Affected units have specific serial numbers.
Lower-risk recall
The CO/CO2 sensor cable harness may have lower electromagnetic shielding, which might have resulted in a non-compliance with the IEC 60601-1-2 standard. As a consequence of a lower electromagnetic shielding provided by the cable harness, the CO/CO2 sensor could have been influenced by high frequencies emitted by very close devices.
Contact the company
What happened, in plain English
NDDd Medical Technologies is recalling EasyOne Pro Respiratory Analysis System Model 3000-1 devices because their CO/CO2 sensor cable may not shield well enough from electromagnetic interference. This could cause inaccurate readings if used near strong electronic devices. Read more at govinfonow.com/recall/73138-easyone-pro-respiratory-device-recall-co-co2-sensor-cable-shielding.
Source Summary by GovInfoNow · govinfonow.com/recall/73138-easyone-pro-respiratory-device-recall-co-co2-sensor-cable-shielding · Updated September 18, 2026 · FDA enforcement record: FDA #Z-0596-2020
Cite this page
“EasyOne Pro Respiratory Device Recall: CO/CO2 Sensor Cable Shielding Issue.” GovInfoNow, updated September 18, 2026. https://govinfonow.com/recall/73138-easyone-pro-respiratory-device-recall-co-co2-sensor-cable-shielding. Based on FDA recall #Z-0596-2020 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0596-2020%22&limit=1).
Why it’s dangerous
The CO/CO2 sensor cable harness has weaker electromagnetic shielding than required. This could allow signals from nearby electronic devices to interfere with the sensor readings, potentially causing inaccurate results during medical tests.
Who’s affected
Healthcare professionals using the EasyOne Pro Model 3000-1 for pulmonary function testing are most at risk. Patients using this device for medical assessments may also be affected.
How to tell if you have this one
Check for the EasyOne Pro Model 3000-1 with serial numbers 550066 through 550072. This device is used for respiratory testing in medical settings.
- Brand
NDDd Medical Technologies- Category
Medical device
All 2 products in this recall
FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.
- Classification
Class II- Status
Terminated- Distribution
The products were distributed to the following US states: KY, MO, NY, OH, PA
| Recall number | Product, codes & lots |
|---|---|
| Z-0596-2020 | EasyOne Pro Respiratory Analysis System Pulmonary Function Testing Device, Model 3000-1; Serial Numbers: 550066 550067 550068 550069 550071 550072 |
| Z-0597-2020 | EasyOne Pro LAB VOS Respiratory Analysis System Pulmonary Function Testing Device, Model 3100-1; Serial Numbers: 650074 650085 650075 650086 650076 650087 650079 650088 650080 650089 650081 650090 650082 650091 650083 650092 650094 650095 650096 650098 650099 650100 650104 650055 650058 650062 650066 650067 650069 650070 650073 |
What to do — step by step
Check Serial Numbers
Verify if your device has serial numbers 550066, 550067, 550068, 550069, or 550071-550072.
Where it went and when
Where it was distributed
Distributed in 5 states.
FDA distribution: “The products were distributed to the following US states: KY, MO, NY, OH, PA” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Kentucky, Missouri, New York, Ohio, Pennsylvania.
Recall timeline
FDA terminated this recall 2.7 years after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
- FDA terminated the recall
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-0596-2020 (August 15, 2017) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0596-2020 to see it in context.
- Plain-language summary written by qwen3:4b on September 18, 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.