FDA recall D-1435-2019
Baxter Healthcare Corporation · Class II · drug
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
- 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
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-1435-2019