FDA recall D-0750-2018
Kroger Specialty Pharmacy, Inc. · Class II · drug
Product
Orkambi 200 mg/125 mg Tablets #112 NDC 51167-0809-01 28 days supply.
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-0750-2018