Central Admixture Pharmacy Services recalls phenylephrine solutions for injection that may not be sterile, posing a risk of infection. Products were distributed to hospitals and clinics. Affected lots have specific expiration dates.
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 solutions for injection that may not be sterile. This could lead to infections if used in medical procedures. Healthcare facilities and patients receiving these products should stop using the affected lots immediately.
The FDA found that the products intended to be sterile may not have been properly sterilized. This lack of sterility can cause infections in medical procedures, especially when used in sensitive environments like hospitals.
Healthcare facilities and medical professionals using the recalled phenylephrine solutions for injection. Patients receiving these products through hospital or clinic care are at risk of infection.
Check the product label for the lot numbers listed: 37-883074 through 37-898523. The expiration dates range from April 28, 2023 to June 29, 2023. These products are for injection only and are used in hospitals and clinics.
Immediately discard any phenylephrine solutions with the listed lot numbers and expiration dates.
The FDA found that the products intended to be sterile may not have been properly sterilized, posing a risk of infection.
Discard the product immediately and contact your healthcare provider for alternative solutions.
Yes, the products have expiration dates ranging from April 28, 2023 to June 29, 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-0733-2023 — Central Admixture Pharmacy Services Central Admixture Pharmacy Services Hello, I own a Central Admixture Pharmacy Services that is covered by recall D-0733-2023 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.
