Class II

Medical Device Recall: Tec 820 ISO Anesthesia Vaporizer, Reference Number 1177-9820-ISO

GE Medical Systems, LLC · November 18, 2024

Reason for Recall

Due to a manufacturing issue, certain Tec 6 Plus and Tec 800 series vaporizers can deliver less anesthetic agent than the vaporizer dial setting.

Distribution

US Nationwide. Global Distribution.

States Affected

NATIONWIDE

Quantity Affected

644 units

Source: FDA (openFDA Device Enforcement)

Recall number: Z-0815-2025

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.

GE Medical Systems, LLC Medical Device Recall: Tec 820 ISO Anesthesia Vaporizer, Reference Number 1177-9820-ISO | SafeCheck