SterRx recalls 150 mEq per 1000 mL Sodium Bicarbonate in 5% Dextrose Injection (Rx only) due to lack of sterility assurance. This may cause infections if used improperly.
Lack of Assurance of Sterility
SterRx is recalling a specific type of IV solution that may not be sterile, which could lead to infections if used in medical treatments. Patients and healthcare providers should check if they have this product and take appropriate action.
The product lacks assurance of sterility, meaning it could contain harmful bacteria or other contaminants. If this solution is used in medical procedures, it might cause infections or other health issues.
People who have been prescribed this medication by a doctor or healthcare provider. Those using it for medical treatments are at risk of infection if the product is not sterile.
Check for the product name: Sodium Bicarbonate in 5% Dextrose Injection, 150 mEq per 1000 mL (12.6 mg per mL). It was sold by SterRx, LLC with NDC 70324-326-01. The product was manufactured between November 2021 and July 2022.
Identify if you have the specific Sodium Bicarbonate in 5% Dextrose Injection with NDC 70324-326-01.
The recall states there is a lack of assurance of sterility, so it may not be safe to use. Do not use this product without checking with your healthcare provider.
Look for the product name: Sodium Bicarbonate in 5% Dextrose Injection, 150 mEq per 1000 mL (12.6 mg per mL), with NDC 70324-326-01. It was manufactured between November 2021 and July 2022.
The recall does not specify a remedy, so contact your healthcare provider for guidance on whether to stop using it or return it.
We’ve drafted a message you can send SterRx to request your refund or repair — edit it as you like.
Subject: Recall D-0306-2022 — SterRx SterRx Hello, I own a SterRx that is covered by recall D-0306-2022 from SterRx. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
