Class II

Medical Device Recall: Tec 850 ISO Anesthesia Vaporizer, Reference Number 1177-9850-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

1594 units

Source: FDA (openFDA Device Enforcement)

Recall number: Z-0817-2025

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.