US Drug Recall Register
Class II · Moderate risk Terminated 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.

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