Central Admixture Pharmacy Services recalls phenylephrine 50mg in 0.9% sodium chloride solution (NDC 71285-7039-1) due to potential lack of sterility after FDA inspection. Affected lots expire May 2023.
Lack of Assurance of Sterility: after an FDA inspection called into question the sterility of the products intended to be sterile.
Central Admixture Pharmacy Services has recalled phenylephrine 50 mg added to 0.9% sodium chloride 250 mL solutions because an FDA inspection raised concerns about their sterility. This could lead to infections if the solution is not properly sterile.
The FDA inspection found potential issues with the sterility of these solutions. If the solution is not sterile, it could cause infections when administered to patients through intravenous lines.
Healthcare professionals using these solutions for patient medication in hospitals or clinics. Patients receiving these medications through intravenous administration are at risk if the solution is not sterile.
Check for the NDC number 71285-7039-1 on the packaging. Look for lot numbers 37-887056, 37-887057, 37-887059 (expiring May 2023) or 37-893807, 37-896880 (expiring June 2023).
Verify the NDC number 71285-7039-1 and lot numbers listed in the recall notice.
The FDA inspection raised concerns about sterility, so these products should not be used until the recall is resolved.
Contact Central Admixture Pharmacy Services at 6580 Snowdrift Rd., Ste 100, Allentown, PA 18106 for instructions.
Check the NDC number 71285-7039-1 and lot numbers 37-887056, 37-887057, 37-887059 (expiring May 2023) or 37-893807, 37-896880 (expiring June 2023).
We’ve drafted a message you can send Central Admixture Pharmacy Services to request your refund or repair — edit it as you like.
Subject: Recall D-0735-2023 — Central Admixture Pharmacy Services Central Admixture Pharmacy Services Hello, I own a Central Admixture Pharmacy Services that is covered by recall D-0735-2023 from Central Admixture Pharmacy Services. 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.
