Ventec Life Systems, Inc.: Ventilator, Continuous, Facility Use
Recall Summary Ventec Life Systems is recalling VOCSN+Pro ventilators used in medical facilities because some units may have a defective backup battery that prevents the backup alarm from sounding during a power loss. This could delay caregivers from noticing a hazardous situation. The affected ventilators were distributed across the United States.
- Recalling firm
- 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
- Category
- medical device recall
- Country
- United States
- Agency
- FDA-DEVICES
- Recall date
- 2026-05-08
- Status
- Open, Classified
- Areas affected
- AL, AK, AZ, AR, CA, CO, CT, DE, FL, GA, HI, ID, ...
- Distribution
- US Nationwide distribution in the state of UT.
Official recall notice from FDA-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/0f8dbaaf-c624-47e5-b618-98ddb3beab58