Recall Atlas

Ventec Life Systems recalls

5 official recalls and safety alerts involving Ventec Life Systems since 2024-03, from FDA · Device. Newest first. Check the official notice for exact models and batch codes.

This list only includes recalls Recall Atlas has collected since 2021-10. A product not listed here may still be affected; check with Ventec Life Systems or the relevant agency.

  1. 2026-09-30
  2. US
    Drugs & medicalClass II

    Ventec Life Systems, Inc. recalls REF: HF2POSTD HomeFill Oxygen System HomeFill cylinder D with CGA870 Compatible Post Valve

    Labeling; Oxygen Cylinders do not contain required medical gas labeling

    FDA · DeviceVentec Life Systems, Inc.US Nationwide distribution in the states of FL, IA, OH, NE, TN.Official notice →
  3. 2026-07-01
  4. US
    Drugs & medicalClass II

    Ventec Life Systems, Inc. recalls VOCSN+Pro package, REF: PRT-00853-000; VOCSN+Pro unit, REF: PRT-00490-001

    Respiratory system intended to provide continuous/intermittent ventilator support, may have a damaged back-up battery supporting backup alarm function, which may result in the backup alarm not activating during loss of…

    FDA · DeviceVentec Life Systems, Inc.US Nationwide distribution in the state of UT.Official notice →
  5. 2026-05-13
  6. US
    Drugs & medicalClass I

    Ventec Life Systems, Inc. recalls VOCSN V+Pro package, REF: PRT-01198-000; VOCSN V+Pro unit, REF: PRT-01185-000

    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…

    FDA · DeviceVentec Life Systems, Inc.US: OH, GA, CA, MOOfficial notice →
  7. 2025-03-05
  8. US
    Drugs & medicalClass I

    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: PRT-01185-000,…

    Multi-Function Ventilators were serviced using incorrect parts which have the potential to cause unexpected shutdown, or when using an active circuit could result in inaccurate tidal volume monitor, not triggering on…

    FDA · DeviceVentec Life Systems, Inc.US distribution in CA, NY, and MO.Official notice →
  9. 2024-03-06
  10. US
    Drugs & medicalClass I

    Ventec Life Systems, Inc. recalls VOCSN Patient Breathing Package (Pediatric, Active, Oxygen, Blue) REF PRT-01013-000 with pouch REF PRT-00802-001). Used with the VOCSN…

    The bonded spiral wrap may detach before or during ventilation due to a manufacturing issue. Detachment of the spiral wrap can compromise structural integrity, functionality and/ or performance resulting in occlusions…

    FDA · DeviceVentec Life Systems, Inc.U.S.: CA, CO, FL, HI, IN, MO, NC, and WA O.U.S.: JapanOfficial notice →