SterRx recalls morphine sulfate injections due to lack of sterility assurance. This could cause infections if used improperly. Affected products have specific NDC numbers and were sold in New York.
Lack of Assurance of Sterility
SterRx is recalling morphine sulfate injections that may not be sterile, which could lead to infections if used. This is a serious safety issue for patients receiving the medication.
The injections lack assurance of sterility, meaning they could contain harmful bacteria or other contaminants. If used, this could cause serious infections, especially in patients with weakened immune systems or open wounds.
Patients prescribed morphine sulfate injections by a healthcare provider are affected. Those using the recalled product without medical supervision are at risk of infection.
Check for the NDC number 70324-427-01 on the product label. The product was manufactured by SterRx in Plattsburgh, NY and sold as a prescription-only injection.
Immediately stop using the recalled morphine sulfate injection if you have it.
No, the product lacks sterility assurance and could cause infections. Do not use it.
Stop using it immediately and contact your healthcare provider for alternative treatment.
Look for the NDC number 70324-427-01 on the label. The product was sold by SterRx in Plattsburgh, NY.
We’ve drafted a message you can send SterRx to request your refund or repair — edit it as you like.
Subject: Recall D-0318-2022 — SterRx SterRx Hello, I own a SterRx that is covered by recall D-0318-2022 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.
