Class III · Low risk Terminated
Milrinone Lactate Injection
Reason Failed Impurities/Degradation Specifications
Milrinone 200 mcg/mL in a) D5W-300 mL
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Why it was recalled
Lack of Sterility Assurance
What was recalled
Milrinone 200 mcg/mL in a) D5W-300 mL, b) D5W-400 mL, c) D5W-500 mL and d) D5W-600 mL Bags, FOR IV USE ONLY, Baptist Health Medical Towers Pharmacy & Infusion, Little Rock, AR
- Recalling firm
- Baptist Health Medical Towers Pharmacy and Infusion Services
- Origin
- AR, United States
- Initiated by
- Voluntary: Firm initiated
- FDA recall number
- D-0930-2016
What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.
Other Milrinone recalls
See all
Class II · Moderate risk Terminated
Milrinone
Reason Lack of sterility assurance
Class II · Moderate risk Terminated
Milrinone Lactate Injection 200 mcg
Reason Lack of Assurance of Sterility: Bags have the potential to leak.
Class II · Moderate risk Terminated
Milrinone Lactate Injection 200 mcg
Reason Lack of Assurance of Sterility: Bags have the potential to leak.
Class II · Moderate risk Terminated
Milrinone Lactate in 5% Dextrose Injection
Reason Lack of assurance of sterility: customer complaints received for the presence of leaks.
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