Class II

Medical Device Recall: AW Server 2.0, AW Server 3.0, AW Server 3.1, AW Server 3.2

GE Medical Systems, SCS · September 5, 2025

Reason for Recall

Firm has identified a security vulnerability in AW Server products. If exploited, a malicious actor could compromise the confidentiality, integrity, and availability of patient data.

Distribution

Domestic US distribution nationwide. International distribution worldwide.

States Affected

NATIONWIDE

Quantity Affected

7,302 (1,381 US; 5,921 OUS)

Source: FDA (openFDA Device Enforcement)

Recall number: Z-0068-2026

Status: ongoing

SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.