PlainRecalls
FDA Devices Moderate Class II Ongoing

The Pressio 2 ICP Monitoring System, Model Number PSO-4000; Intracranial Pressure Monitor

Reported: January 14, 2026 Initiated: November 17, 2025 #Z-1029-2026

Product Description

The Pressio 2 ICP Monitoring System, Model Number PSO-4000; Intracranial Pressure Monitor

Reason for Recall

Customer complaints of Pressio monitor rebooting.

Details

Recalling Firm
Sophysa
Units Affected
105 units
Distribution
US Nationwide distribution in the states of AZ, WI, TX, OR, CA, OK, ID, FL, NJ.
Location
Besancon

Frequently Asked Questions

What product was recalled?
The Pressio 2 ICP Monitoring System, Model Number PSO-4000; Intracranial Pressure Monitor. Recalled by Sophysa. Units affected: 105 units.
Why was this product recalled?
Customer complaints of Pressio monitor rebooting.
Which agency issued this recall?
This recall was issued by the FDA Devices on January 14, 2026. Severity: Moderate. Recall number: Z-1029-2026.