Use cautionMedical device recall · FDA · Published March 25, 2026
Ventec V+Pro Ventilator Recall: Oxygen Leak Risk
Ventec Life Systems recalls V+Pro ventilators with specific serial numbers due to potential oxygen leaks that could reduce oxygen delivery and increase fire risk. Affected units must be checked for serial numbers listed in the recall notice.
Respiratory system intended to provide continuous/intermittent ventilator support, may not have been evaluated under all intended high-pressure conditions during production testing, so an oxygen leak condition could occur that may lead to reduced below intended levels of fraction of inspired oxygen delivery prior to and during ventilation and this oxygen-enriched environment may increase fire risk
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Contact the company
📍Recalling firmVentec Life Systems, Inc.22002 26th Ave Se · Bothell, WA 98021-4903
✎ GovInfoNow plain-language explainer
Ventec Life Systems is recalling V+Pro ventilators that may have oxygen leaks, which could lower oxygen delivery during ventilation and create a fire risk. This recall affects specific units with listed serial numbers and requires immediate attention to prevent potential harm. Read more at govinfonow.com/recall/49602-ventec-v-pro-ventilator-recall-oxygen-leak-risk.
“Ventec V+Pro Ventilator Recall: Oxygen Leak Risk.” GovInfoNow, updated August 17, 2026. https://govinfonow.com/recall/49602-ventec-v-pro-ventilator-recall-oxygen-leak-risk. Based on FDA recall #Z-1942-2026 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1942-2026%22&limit=1).
The FDA announced on March 25, 2026, that Ventec Life Systems, Inc. is recalling VOCSN V+Pro packages and units due to a potential oxygen leak that increases fire risk. The agency classified the recall as Class I.
The respiratory system may not have been evaluated under all intended high-pressure conditions during production testing. An oxygen leak condition could occur that may lead to reduced below intended levels of fraction of inspired oxygen delivery prior to and during ventilation. This oxygen-enriched environment may increase fire risk.
Context
GovInfoNow's records show Ventec Life Systems, Inc. has 5 other recalls on record since 2021-05-10. Recent brand recalls include a labeling hazard for the HF2P0ST9 HomeFill Oxygen System (2026-07-28), a backup alarm failure in the VOCSN+Pro Ventilator (2026-05-08), and incorrect parts causing inaccurate monitoring in Multi-Function Ventilators (2025-02-03). Other recent recalls of similar products include the Baxter Blue Ventilator Adapter Module Recall (2026-02-18), ResMed Astral Ventilators Recall (2026-06-25), and Hillrom VOLARA System P.CIRCUIT 5KIT AC Recall (2026-05-21).
How to tell if you have this one
Check for the package serial numbers listed: 152884-152919, 152986-152987, 155236, 156507-156532. The units are sold under the Ventec V+Pro brand with specific reference numbers.
Brand
Ventec Life Systems
Category
Medical device
Based on the official FDA remedy
What to do — step by step
Check Serial Numbers
Look for the package serial numbers listed in the recall notice: 152884-152919, 152986-152987, 155236, 156507-156532.
Where it went and when
Where it was distributed
Distributed in 4 states.
Listed by the agency
Not listed
FDA distribution: “US: OH, GA, CA, MO” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: California, Georgia, Missouri, Ohio.
Recall timeline
FDA published this recall 49 days after the firm started it.
1Firm started the recall
2FDA classified it Class I
3Published in FDA’s Enforcement Report
Dates from the agency record only; steps without a date are left out.
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-1942-2026 (March 25, 2026) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1942-2026 to see it in context.
Plain-language summary written by qwen3:4b on August 17, 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.