SterRx recalls NOREPINEPHRINE 5% Dextrose Injection (8 mg/250mL) due to lack of sterility assurance. This injectable medication may cause infections if used.
Lack of Assurance of Sterility
SterRx is recalling a specific type of injectable medication that could be contaminated, posing infection risks. This recall affects healthcare professionals and patients using this medication under prescription.
The medication lacks assurance of sterility, meaning it could contain harmful bacteria or other contaminants. If injected, this could lead to infections or other health complications.
Healthcare professionals and patients who have been prescribed this injectable medication. Those using it for medical treatments are most at risk.
Check for the product name 'NOREPINEPHRINE in 5% Dextrose Injection, 8 mg per 250 mL (32 mg per mL) Injection, Rx only' from SterRx. The NDC number 70324-476-01 is also associated with this product.
Verify the product name and NDC number to confirm if it matches the recalled item.
The recall indicates a lack of sterility assurance, so it should not be used until the recall is resolved.
The recall record does not specify a replacement process or remedy.
The recall record does not provide specific instructions for affected individuals.
We’ve drafted a message you can send SterRx to request your refund or repair — edit it as you like.
Subject: Recall D-0314-2022 — SterRx SterRx Hello, I own a SterRx that is covered by recall D-0314-2022 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.