Ventec Life Systems, Inc.: Ventilator, Continuous, Facility Use
Recall Summary Ventec Life Systems is recalling the VOCSN+Pro ventilator (Model PRT-00490-100) distributed nationwide because an internal cable connector may disconnect, causing the device to restart and stop delivering ventilation therapy. This affects ventilators used in medical facilities across the United States and Puerto Rico. The company classified this as a Class II recall, indicating a potential serious health risk.
- Recalling firm
- Ventec Life Systems, Inc.
- Product
- VOCSN+Pro (Japan), Model Number: PRT-00490-100, Package PN:PRT-00853-100. used for ventilatory support.
- Reason
- Ventilator's Internal Flow transducer cable connector may disconnect from internal board, potentially resulting in system reboot and interruption of ventilation therapy.
- Classification
- Class II
- Category
- medical device recall
- Country
- United States
- Agency
- FDA-DEVICES
- Recall date
- 2026-09-17
- Status
- Open, Classified
- Areas affected
- AL, AK, AZ, AR, CA, CO, CT, DE, FL, GA, HI, ID, ...
- Distribution
- Distribution US nationwide including Puerto Rico.
Official recall notice from FDA-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/770e5f69-675f-4369-872d-3750e7be66f0