PlainRecalls
FDA Devices Moderate Class II Ongoing

Tec 820 ISO Anesthesia Vaporizer, Reference Number 1177-9820-ISO

Reported: January 15, 2025 Initiated: November 18, 2024 #Z-0815-2025

Product Description

Tec 820 ISO Anesthesia Vaporizer, Reference Number 1177-9820-ISO

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.

Details

Recalling Firm
GE Medical Systems, LLC
Units Affected
644 units
Distribution
US Nationwide. Global Distribution.
Location
Waukesha, WI

Frequently Asked Questions

What product was recalled?
Tec 820 ISO Anesthesia Vaporizer, Reference Number 1177-9820-ISO. Recalled by GE Medical Systems, LLC. Units affected: 644 units.
Why was this product recalled?
Due to a manufacturing issue, certain Tec 6 Plus and Tec 800 series vaporizers can deliver less anesthetic agent than the vaporizer dial setting.
Which agency issued this recall?
This recall was issued by the FDA Devices on January 15, 2025. Severity: Moderate. Recall number: Z-0815-2025.