Class II · Moderate riskTerminated Initiated Jun 13, 2019 (7 years ago)
Sevoflurane, USP Inhalation Anesthetic 250 mL bottles, Rx only, Manufactured for Baxter…
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Why it was recalled
Failed Stability Specifications
What was recalled
Sevoflurane, USP Inhalation Anesthetic 250 mL bottles, Rx only, Manufactured for Baxter Healthcare Corporation Deerfield, IL 60015 USA, NDC 10019-651-64
Recalling firm
Baxter Healthcare Corporation
NDC code
10019-651-64
Origin
IL, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-1435-2019
What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.