Ventec Life Systems, Inc. recalls
Every recall we track for Ventec Life Systems, Inc. — 8 in all, from 2021–2026 — plus the complaints and injury reports the public filed about them. 2 are rated “stop using now”.
Recalls per year, by danger level
8 recalls since 2017. 25% rated “stop using now”.
All FDA recall records for Ventec Life Systems, Inc. since 2017, counted by recall date (one bar per calendar year; 2026 is partial). Danger level is GovInfoNow’s plain-language rating; “not yet rated” records are still being written up.
| Year | Stop using now | Use caution | Lower risk | Not yet rated | Total |
|---|---|---|---|---|---|
| 2017 | 0 | 0 | 0 | 0 | 0 |
| 2018 | 0 | 0 | 0 | 0 | 0 |
| 2019 | 0 | 0 | 0 | 0 | 0 |
| 2020 | 0 | 0 | 0 | 0 | 0 |
| 2021 | 1 | 0 | 0 | 0 | 1 |
| 2022 | 0 | 0 | 0 | 0 | 0 |
| 2023 | 0 | 0 | 0 | 0 | 0 |
| 2024 | 1 | 0 | 0 | 0 | 1 |
| 2025 | 0 | 1 | 0 | 0 | 1 |
| 2026 (to date) | 0 | 2 | 1 | 2 | 5 |
Most common reasons for Ventec Life Systems, Inc. recalls
What to do if you have a recalled Ventec Life Systems, Inc. product
- Match the model, catalog or lot number on your device to the recall.
- Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals.
- Report problems to FDA MedWatch.
All Ventec Life Systems, Inc. recalls
6 shown- Lower riskMedical device
Ventec Life Systems, Inc. recalls REF: HF2POSTD HomeFill Oxygen System HomeFill cylinder D with CGA870 Compatible Post Valve
Ventec Life Systems recalls HomeFill oxygen cylinders with CGA870 Post Valve that lack required medical gas labeling. Consumers should check serial numbers listed to determine if affected.
Ventec Life SystemsJul 28, 2026 - Use cautionMedical device
Ventec Life Systems, Inc. recalls VOCSN+Pro package, REF: PRT-00853-000; VOCSN+Pro unit, REF: PRT-00490-001
Ventec Life Systems recalls VOCSN+Pro ventilators with potential backup alarm failure during power loss. Affected units may not alert caregivers if primary power fails, risking delayed response to hazardous conditions.
Ventec Life SystemsMay 8, 2026 - Use cautionMedical device
Ventec Life Systems, Inc. recalls VOCSN V+Pro package, REF: PRT-01198-000; VOCSN V+Pro unit, REF: PRT-01185-000
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.
Ventec Life SystemsMar 25, 2026 - Use cautionMedical device
Ventec Life Systems, Inc. recalls VOCSN Multi-Function Ventilators: VOCSN+Pro (V+O+C+S+N+Pro, English), REF: PRT-00490-001; V+Pro (V+Pro, English), REF:
Ventec Life Systems recalls VOCSN+Pro and V+Pro ventilators with incorrect parts that could cause inaccurate tidal volume monitoring and unexpected shutdowns. Affected units have specific serial numbers and model references.
Ventec Life SystemsFeb 3, 2025 - Stop using nowMedical device
Ventec Life Systems, Inc. recalls VOCSN Patient Breathing Package (Pediatric, Active, Oxygen, Blue) REF PRT-01013-000 with pouch REF PRT-00802-001). Used
Ventec recalls pediatric oxygen breathing packages with spiral wrap that may detach during use, risking leaks or occlusions that could cause serious injury or death, especially for ventilator-dependent patients.
VentecJan 9, 2024 - Stop using nowMedical device
Ventec Life Systems, Inc. recalls Ventec Life Systems VOCSN Multi-Function Ventilator Model/Version/Catalog Number: V+O+C+S+N+Pro/English/PRT-00490-001;
Ventec Life Systems recalls specific models of VOCSN Multi-Function Ventilators due to potential unexpected shutdowns during patient use, which may prevent ventilation therapy. Affected units include various model numbers and serial numbers listed in the recall notice.
Ventec Life SystemsMay 10, 2021
Ventec Life Systems, Inc. recall questions
How many recalls has Ventec Life Systems, Inc. had?
8 recalls from Ventec Life Systems, Inc. are on record with U.S. safety agencies, from 2021–2026.
What is the most recent Ventec Life Systems, Inc. recall?
Ventec Life Systems, Inc. recalls REF: HF2POSTD HomeFill Oxygen System HomeFill cylinder D with CGA870 Compatible Post Valve, dated Jul 28, 2026. Every Ventec Life Systems, Inc. recall is listed on this page, newest first.
Why are Ventec Life Systems, Inc. products recalled?
The most common reasons on record: Labeling; Oxygen Cylinders do not contain required medical gas labeling (3).
What should I do if I have a recalled Ventec Life Systems, Inc. product?
Match the model, catalog or lot number on your device to the recall. Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals. Report problems to FDA MedWatch.
How do I get alerts for new Ventec Life Systems, Inc. recalls?
Sign up for free email alerts on GovInfoNow — we check official CPSC, FDA, USDA and NHTSA data every day and email you only when a recall matches what you follow.