Baxter International Inc. recalls Baxter — intravenous (IV) solutions: 0.9% Sodium Chloride Injection, USP, 250 mL VIAFLEX Plastic Containe…
- Recall date
- February 8, 2018
- Source
- U.S. Food & Drug Administration (FDA) — recall announcement
- Brand / firm
- Baxter International Inc., Baxter
Why it was recalled
Labeled as Eliquis5 mg was found to contain Eliquis 2.5 mg tablets — Device & Drug Safety
What was recalled
intravenous (IV) solutions: 0.9% Sodium Chloride Injection, USP, 250 mL VIAFLEX Plastic Container and 70% Dextrose Injection (2000 mL) USP
Read the official recall notice →
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