Drug & medication recalls Moderate risk

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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