SterRx recalls PHENYLephrine HCl injections due to lack of sterility assurance. This risk could lead to infections if used improperly. Affected units have specific NDC numbers and were sold from December 2021 to May 2022.
Lack of Assurance of Sterility
SterRx is recalling certain PHENYLephrine HCl injections because they may not be sterile, which could cause infections if used. This affects patients who received these injections from December 2021 to May 2022.
The injections may not be sterile, meaning they could contain harmful bacteria or other contaminants. If used, this could lead to infections or other health issues, especially in medical settings where sterility is critical.
Patients who received the recalled PHENYLephrine HCl injections from December 2021 to May 2022 are affected. Healthcare providers using these injections for medical treatments are at risk.
Check for the NDC number 70324-901-01 on the product label. The product was sold from December 2021 to May 2022 and distributed through SterRx in Plattsburgh, NY.
Look for the NDC number 70324-901-01 on the injection bottle.
The recall states there is a lack of assurance of sterility, so it is not safe to use without checking the recall status.
The recall does not specify a remedy, so contact SterRx directly for guidance.
The product was first sold in December 2021 based on the recall dates.
We’ve drafted a message you can send SterRx to request your refund or repair — edit it as you like.
Subject: Recall D-0324-2022 — SterRx SterRx Hello, I own a SterRx that is covered by recall D-0324-2022 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.