FDA recall D-0739-2018
Kroger Specialty Pharmacy, Inc. · Class II · drug
Product
Pulmicort Respules 0.5 mg/2mL s, 30 days supply, NDC 00186-1989-04
Reason for recall
Lack of Processing Controls.
Distribution
MS, LA, AR, IL, FL
Key facts
- Status
- Terminated
- Initiation date
- 2018-04-03
- Report date
- 2018-05-16
- Termination date
- 2020-05-07
- Voluntary/Mandated
- Voluntary: Firm initiated
- Location
- Vicksburg, MS, United States
Primary source
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0739-2018