VOCSN+Pro package recall — FDA event 98888

What the official notice recommends

1. On 5/8/2026, recall notices were mailed to customers who were asked to do the following:
2. 1) Immediately discontinue use of affected devices. 2) Inspect current stock, quarantine/segregate any unused affected products, remove affected devices from clinical service and segregate to prevent further use. 3) Use an unaffected ventilator for patient support. 4) If you have distributed or transferred affected devices to other facilities, caregivers, or end users, you must promptly notify them of this recall and provide a copy of this notification. 5) Confirm receipt of this notification letter by returning the enclosed Customer Response Form via email to Ventec-Recall@reacthealth.com
3. Upon receipt of the Customer Response Form, firm will arrange for repair of existing device(s). Return the affected product to React Health
4. If you have any questions, please contact firm at 844-698-6276.

The official notice takes precedence over this summary. Talk to your clinician before changing prescribed therapy.