Milrinone Lactate in 5% Dextrose Injection recalled over sterility concerns
- Recall date
- May 15, 2017
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Official notice title
- Baxter Healthcare Corporation recalls Milrinone Lactate in 5% Dextrose Injection, 20 mg/100 mL, 100 mL Single-Dose Intravia Container bag, Rx only, Baxter He…
- Recall number
- D-0789-2017
- FDA classification
- Class II
- Brand / firm
- Baxter Healthcare Corporation
- Sold / distributed
- US and foreign countries: United Arab Emirates, Colombia, and Canada
Why it was recalled
Lack of assurance of sterility: customer complaints received for the presence of leaks.
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
Milrinone Lactate in 5% Dextrose Injection, 20 mg/100 mL, 100 mL Single-Dose Intravia Container bag, Rx only, Baxter Healthcare Corporation, Deerfield, IL 60015, NDC 0338-6010-48
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