Ventec Life Systems, Inc. recalls VOCSN+Pro package
- Recalling company
- Ventec Life Systems, Inc.
- Product
- VOCSN+Pro package, REF: PRT-00853-000; VOCSN+Pro unit, REF: PRT-00490-001
- Reason
- 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 primary power and absence/depletion of backup power sources, which may result in delayed caregiver awareness of a hazardous condition.
- Classification
- Class II – may cause temporary or medically reversible health consequences
- Recall date
- May 8, 2026
- Reported
- Jul 1, 2026
- Distribution
- US Nationwide distribution in the state of UT.
- Status
- Ongoing
- Quantity
- 1
- Lot / codes
- REF/UDI-DI/Serial Number/Lot: PRT-00853-000/00855573007839/155391P/807138, PRT-00490-001/00855573007792/155391/804613
- Company location
- Bothell, WA
- Recall type
- Voluntary: Firm initiated
- Recall number
- Z-2525-2026
- Agency
- U.S. Food and Drug Administration (FDA)
View official FDA notice ↗ Search recall number Z-2525-2026 in the FDA Enforcement Report. Also see FDA recall press releases.
If you use this product, check the lot, NDC or model number against the official notice and follow its instructions. Do not stop a prescribed medicine or remove a medical device without talking to your doctor or pharmacist. Report problems to FDA MedWatch. FoodRecallNow summarizes public FDA data and is not medical advice.