SterRx recalls Morphine Sulfate injection (100 mg/100 mL) due to lack of sterility assurance. This may cause infections if used improperly.
Lack of Assurance of Sterility
SterRx is recalling Morphine Sulfate injection (100 mg per 100 mL) because it lacks sterility assurance. Using this product could lead to infections, especially in medical settings where sterile injections are critical.
The injection lacks sterility assurance, meaning it could contain harmful bacteria or contaminants. If used improperly, this can cause infections in patients, particularly those with weakened immune systems or undergoing medical procedures.
Healthcare professionals and patients prescribed this medication are affected. Those using the product for pain management are at risk of infection.
Check for the product name 'Morphine Sulfate in 5% Dextrose Injection, 100 mg per 100 mL (1 mg per mL)' with NDC 70324-452-01. It was sold by SterRx in Plattsburgh, NY.
Look for the NDC code 70324-452-01 on the product label.
The recall states there is a lack of sterility assurance, so it is not safe to use. The product should be discontinued.
The recall does not specify a remedy, so contact your healthcare provider for guidance.
Check the product label for NDC 70324-452-01 and the description 'Morphine Sulfate in 5% Dextrose Injection, 100 mg per 100 mL (1 mg per mL)'.
We’ve drafted a message you can send SterRx to request your refund or repair — edit it as you like.
Subject: Recall D-0313-2022 — SterRx SterRx Hello, I own a SterRx that is covered by recall D-0313-2022 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.
