# FDA recall Z-0814-2025

> **GE Medical Systems, LLC** · Class II · device recall initiated 2024-11-18.

## Product

Tec 6 Plus Anesthesia Vaporizer, Reference Numbers 1107-9601-000, 1107-9602-000, 1107-9603-000, 1107-9604-000, 1107-9610-000, 1107-9612-000, 1107-9616-000, 1107-9617-000, 2066835-001, 2069767-001, 2078800-001, 2091008-001, 2091009-001, M1098876, M1145610, M1220023, M1220854, M1221495, and M1233992

## 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.

## Key facts

- **Recall number:** Z-0814-2025
- **Recalling firm:** GE Medical Systems, LLC
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2024-11-18
- **Report date:** 2025-01-15

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Waukesha, WI, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0814-2025

## Citation

> AI Analytics. FDA recall Z-0814-2025. Retrieved 2026-07-27 from https://api.ai-analytics.org/recall/Z-0814-2025. Source: US FDA. Licensed CC0.

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