Sodium Bicarbonate in 5% Dextrose Injection recalled over sterility concerns
- Recall date
- July 7, 2023
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Official notice title
- SterRx, LLC recalls Sodium Bicarbonate in 5% Dextrose Injection, 150 mEq per 1,000 mL (12.6 mg per mL), 1,000 mL Single Dose bag, packaged…
- Recall number
- D-0930-2023
- FDA classification
- Class II
- Brand / firm
- SterRx, LLC
- Sold / distributed
- Nationwide in the USA
Why it was recalled
Lack of Assurance of Sterility
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
Sodium Bicarbonate in 5% Dextrose Injection, 150 mEq per 1,000 mL (12.6 mg per mL), 1,000 mL Single Dose bag, packaged in 1000 mL x 6 units per case, SterRx, 141 Idaho Ave., Plattsburgh, NY 12903, NDC 70324-326-01.
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