SterRx recalls Morphine Sulfate injection (100 mg/100mL) due to lack of sterility assurance. This could cause infections if used improperly.
Lack of Assurance of Sterility
SterRx is recalling Morphine Sulfate injection (100 mg per 100 mL) because it may not be sterile. Using this product could lead to infections, especially in medical settings where sterility is critical.
The product lacks assurance of sterility, meaning it could contain harmful bacteria or contaminants. If this injection is used without proper sterilization, it might cause infections in patients.
Healthcare professionals and patients who have been prescribed this morphine injection. Those using it for pain management in medical settings are most at risk.
Check for the product name 'Morphine Sulfate in 0.9% Sodium Chloride Injection, 100 mg per 100 mL (1 mg per mL)' with the NDC code 70324-427-02. It was sold by SterRx in Plattsburgh, NY.
Look for the NDC code 70324-427-02 on the product label to confirm it is the recalled item.
The recall states there is a lack of assurance of sterility, so it is not safe to use without the remedy.
The recall record does not specify a remedy, so replacement is not mentioned.
The product may not be sterile, which could lead to infections if used improperly.
We’ve drafted a message you can send SterRx to request your refund or repair — edit it as you like.
Subject: Recall D-0301-2022 — SterRx SterRx Hello, I own a SterRx that is covered by recall D-0301-2022 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.
