Ventec Life Systems, Inc. 2026-07-01 Health serious FDA
Health · FDA · Recall #FDA-Z-2525-2026
VOCSN+Pro package, REF: PRT-00853-000; VOCSN+Pro unit, REF: PRT-00490-001 Recall
Issued July 1, 2026 · Ventec Life Systems, Inc.
In July 2026, Ventec Life Systems, Inc. recalled the VOCSN+Pro package, REF: PRT-00853-000; VOCSN+Pro unit, REF: PRT-00490-001, a serious health recall reported by the FDA.
Compiled by Dana Whitfield, RecallCheckr
What this means for you
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.
What you should do
- 1 Stop using VOCSN+Pro package, REF: PRT-00853-000; VOCSN+Pro unit, REF: PRT-00490-001 right away.
- 2 Set it aside where it won't be used by mistake.
- 3 Contact Ventec Life Systems, Inc. to arrange your voluntary. See the official notice below for contact details.
- 4 Keep the product until your remedy is fully processed. You may need it.
Official remedy (Voluntary):
Recall details
- Brand
- Ventec Life Systems, Inc.
- Category
- Health
- Recall date
- July 1, 2026
- Units affected
- Not reported
- Sold at
- US Nationwide distribution in the state of UT.
- Recall number
- FDA-Z-2525-2026
- Made in
- United States
- Issuing agency
- FDA
In context
- Ventec Life Systems, Inc. has 1 recall in our database.
- We're tracking 3,673 Health recalls in our database.
- This is the 453rd Health recall we've logged in 2026.