# FDA recall D-1435-2019

> **Baxter Healthcare Corporation** · Class II · drug recall initiated 2019-06-13.

## Product

Sevoflurane, USP Inhalation Anesthetic 250 mL bottles, Rx only, Manufactured for Baxter Healthcare Corporation Deerfield, IL 60015 USA, NDC 10019-651-64

## Reason for recall

Failed Stability Specifications

## Distribution

Nationwide within the United States

## Key facts

- **Recall number:** D-1435-2019
- **Recalling firm:** Baxter Healthcare Corporation
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2019-06-13
- **Report date:** 2019-06-19
- **Termination date:** 2020-04-29

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Deerfield, IL, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-1435-2019

## Citation

> AI Analytics. FDA recall D-1435-2019. Retrieved 2026-07-10 from https://api.ai-analytics.org/recall/D-1435-2019. Source: US FDA. Licensed CC0.

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