Hospira Inc, A Pfizer Company recalls Hospira — 8.4% Sodium Bicarbonate Injection, USP, NeutTM (Sodium Bicarbonate 4% additive solution), Q…
- Recall date
- February 6, 2018
- Source
- U.S. Food & Drug Administration (FDA) — recall announcement
- Brand / firm
- Hospira Inc, A Pfizer Company, Hospira
Why it was recalled
Due to microbial growth — Device & Drug Safety
What was recalled
8.4% Sodium Bicarbonate Injection, USP, NeutTM (Sodium Bicarbonate 4% additive solution), QUELICINTM (Succinylcholine Chloride Injection, USP) and Potassium Phosphates Injection, USP
Read the official recall notice →
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