Drug Recall Terminated Historical recordClass II
Cyclophosphamide 50 mg cap NDC 00054-0383-25 28 days supply
- Reason
- Lack of Processing Controls.
- Recall initiated
- April 3, 2018
- Reported by FDA
- May 16, 2018
- Distribution
- MS, LA, AR, IL, FL
FDA Drug Recalls
Every FDA drug enforcement recall Public Health Trace has on record, republished from openFDA's official drug enforcement database. See Health Alerts for current, active recalls alongside outbreaks and advisories.
Drug recall information is sourced from the FDA's structured openFDA Enforcement Reports. Newly announced recalls may appear on FDA.gov before they become available in the structured dataset. See Methodology for how Public Health Trace imports and refreshes this data.
Filters
Drug Recall Terminated Historical recordClass II
Sprycel 100 mg tablet NDC 00003-0852-22 30 days supply
- Reason
- Lack of Processing Controls.
- Recall initiated
- April 3, 2018
- Reported by FDA
- May 16, 2018
- Distribution
- MS, LA, AR, IL, FL
Drug Recall Terminated Historical recordClass II
Sprycel 80 mg tablet NDC 00003-0855-22 30 days supply
- Reason
- Lack of Processing Controls.
- Recall initiated
- April 3, 2018
- Reported by FDA
- May 16, 2018
- Distribution
- MS, LA, AR, IL, FL
Drug Recall Terminated Historical recordClass II
Gleevec 100 mg tablet NDC 00078-0401-34 30 days supply
- Reason
- Lack of Processing Controls.
- Recall initiated
- April 3, 2018
- Reported by FDA
- May 16, 2018
- Distribution
- MS, LA, AR, IL, FL
Drug Recall Terminated Historical recordClass II
Temozolomide 250 mg NDC 43975-0257-05 28 days supply
- Reason
- Lack of Processing Controls.
- Recall initiated
- April 3, 2018
- Reported by FDA
- May 16, 2018
- Distribution
- MS, LA, AR, IL, FL
Drug Recall Terminated Historical recordClass II
Temozolomide 20 mg NDC 43975-0253-05 28 days supply
- Reason
- Lack of Processing Controls.
- Recall initiated
- April 3, 2018
- Reported by FDA
- May 16, 2018
- Distribution
- MS, LA, AR, IL, FL
Drug Recall Terminated Historical recordClass II
Xalkori 250 mg cap NDC 00069-8140-20 30 days supply
- Reason
- Lack of Processing Controls.
- Recall initiated
- April 3, 2018
- Reported by FDA
- May 16, 2018
- Distribution
- MS, LA, AR, IL, FL
Drug Recall Terminated Historical recordClass II
Glatiramer Acetate 40 mg/mL NDC 00378-6961-12 28 days supply
- Reason
- Lack of Processing Controls.
- Recall initiated
- April 3, 2018
- Reported by FDA
- May 16, 2018
- Distribution
- MS, LA, AR, IL, FL
Drug Recall Terminated Historical recordClass II
Ibrance 125 mg cap NDC 00069-0189-21 28 days supply
- Reason
- Lack of Processing Controls.
- Recall initiated
- April 3, 2018
- Reported by FDA
- May 16, 2018
- Distribution
- MS, LA, AR, IL, FL
Drug Recall Terminated Historical recordClass II
Avonex 30 mcg/0.5 mL PFS Kit NDC 59627-0222-05 28 days supply
- Reason
- Lack of Processing Controls.
- Recall initiated
- April 3, 2018
- Reported by FDA
- May 16, 2018
- Distribution
- MS, LA, AR, IL, FL
Drug Recall Terminated Historical recordClass II
Revlimid 25 mg oral cap NDC 59572-0425-21 28 days supply
- Reason
- Lack of Processing Controls.
- Recall initiated
- April 3, 2018
- Reported by FDA
- May 16, 2018
- Distribution
- MS, LA, AR, IL, FL
Drug Recall Terminated Historical recordClass II
Revlimid 5 mg oral cap NDC 59572-0405-28 28 days supply
- Reason
- Lack of Processing Controls.
- Recall initiated
- April 3, 2018
- Reported by FDA
- May 16, 2018
- Distribution
- MS, LA, AR, IL, FL
Drug Recall Terminated Historical recordClass II
Revlimid 20 mg oral cap NDC 59572-0420-21 28 days supply
- Reason
- Lack of Processing Controls.
- Recall initiated
- April 3, 2018
- Reported by FDA
- May 16, 2018
- Distribution
- MS, LA, AR, IL, FL
Drug Recall Terminated Historical recordClass II
Revlimid 15 mg oral cap NDC 59572-0415-21 28 days supply
- Reason
- Lack of Processing Controls.
- Recall initiated
- April 3, 2018
- Reported by FDA
- May 16, 2018
- Distribution
- MS, LA, AR, IL, FL
Drug Recall Terminated Historical recordClass II
Revlimid 10 mg oral cap NDC 59572-0410-28 28 days supply
- Reason
- Lack of Processing Controls.
- Recall initiated
- April 3, 2018
- Reported by FDA
- May 16, 2018
- Distribution
- MS, LA, AR, IL, FL
Drug Recall Terminated Historical recordClass II
Promacta 50 mg tablet NDC 00078-0686-15 30 days supply
- Reason
- Lack of Processing Controls.
- Recall initiated
- April 3, 2018
- Reported by FDA
- May 16, 2018
- Distribution
- MS, LA, AR, IL, FL
Drug Recall Terminated Historical recordClass II
Xtandi 40 mg capsule NDC 00469-0125-99 30 days supply
- Reason
- Lack of Processing Controls.
- Recall initiated
- April 3, 2018
- Reported by FDA
- May 16, 2018
- Distribution
- MS, LA, AR, IL, FL
Drug Recall Terminated Historical recordClass II
Pomalyst 3 mg capsule NDC 59572-0503-21 28 days supply
- Reason
- Lack of Processing Controls.
- Recall initiated
- April 3, 2018
- Reported by FDA
- May 16, 2018
- Distribution
- MS, LA, AR, IL, FL
Drug Recall Terminated Historical recordClass II
Tecfidera 240 mg capsule NDC 64406-0006-02 30 days supply
- Reason
- Lack of Processing Controls.
- Recall initiated
- April 3, 2018
- Reported by FDA
- May 16, 2018
- Distribution
- MS, LA, AR, IL, FL
Drug Recall Terminated Historical recordClass II
Copaxone 20 mg Injection PFS (30) NDC 68546-0317-30 30 days supply.
- Reason
- Lack of Processing Controls.
- Recall initiated
- April 3, 2018
- Reported by FDA
- May 16, 2018
- Distribution
- MS, LA, AR, IL, FL
Data last updated:
This information is republished from FDA's Recall Enterprise System through openFDA. Public Health Trace does not verify or supplement it, is not affiliated with the FDA, and does not provide medical advice -- always follow the guidance of your pharmacist, physician, or the recalling company for any medication you take. Read the full medical disclaimer.
