# FDA recall Z-0818-2025

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

## Product

Tec 850 SEV Anesthesia Vaporizer, Reference Number 1177-9850-SEV

## 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-0818-2025
- **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-0818-2025

## Citation

> AI Analytics. FDA recall Z-0818-2025. Retrieved 2026-07-20 from https://api.ai-analytics.org/recall/Z-0818-2025. Source: US FDA. Licensed CC0.

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*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*