SterRx recalls specific PHENYLepherine HCl solution due to lack of sterility assurance. This Rx-only medication may pose infection risks if used improperly.
Lack of Assurance of Sterility
SterRx is recalling a specific prescription PHENYLepherine HCl solution because it lacks sterility assurance. This could lead to infections if the medication is used without proper sterilization.
The medication lacks sterility assurance, meaning it could be contaminated with bacteria or other pathogens. This poses a risk of infection if the solution is used without proper sterilization procedures.
Prescription patients who have received this specific PHENYLepherine HCl solution from SterRx. Those with medical conditions requiring this medication are most at risk.
Check for the product name PHENYLepherine HCL in 0.9% Sodium Chloride, 20 mg per 250 mL (80 mcg per mL). It was sold by SterRx, LLC in Plattsburgh, NY with NDC 70324-701-01.
Verify the product name, concentration, and NDC number to confirm if it matches the recalled items.
The recall states there is a lack of sterility assurance, so it may pose infection risks. Do not use until you confirm it is not recalled.
Check for the product name PHENYLepherine HCL in 0.9% Sodium Chloride, 20 mg per 250 mL (80 mcg per mL) with NDC 70324-701-01.
The recall does not specify a remedy, so contact SterRx directly for guidance on next steps.
We’ve drafted a message you can send SterRx to request your refund or repair — edit it as you like.
Subject: Recall D-0305-2022 — SterRx SterRx Hello, I own a SterRx that is covered by recall D-0305-2022 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.
