FDA Drug Moderate Class II Terminated

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

Reported: June 19, 2019 Initiated: June 13, 2019 #D-1435-2019

Product Description

Reason for Recall

Failed Stability Specifications

Details

Recalling Firm: Baxter Healthcare Corporation
Units Affected: 5940 bottles
Distribution: Nationwide within the United States
Location: Deerfield, IL

Frequently Asked Questions

What product was recalled? ▼

Sevoflurane, USP Inhalation Anesthetic 250 mL bottles, Rx only, Manufactured for Baxter Healthcare Corporation Deerfield, IL 60015 USA, NDC 10019-651-64. Recalled by Baxter Healthcare Corporation. Units affected: 5940 bottles.

Why was this product recalled? ▼

Failed Stability Specifications

Which agency issued this recall? ▼

This recall was issued by the FDA Drug on June 19, 2019. Severity: Moderate. Recall number: D-1435-2019.