Central Admixture Pharmacy Services recalls oxyTOCIN 15 units added to 0.9% sodium chloride 250 mL per bag due to lack of sterility assurance after FDA inspection. Products may not be sterile and could cause infections.
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 is recalling oxyTOCIN 15 units added to 0.9% sodium chloride 250 mL per bag because an FDA inspection raised concerns about sterility. This could lead to infections if the product is not properly sterile.
The FDA inspection found that the products intended to be sterile may not have been properly sterilized. This lack of sterility could lead to infections if the product is used in medical procedures.
Healthcare providers and patients who have received this specific oxyTOCIN product from Central Admixture Pharmacy Services. Those using the product for medical purposes are at risk of infection.
Check for the product name 'oxyTOCIN 15 units added to 0.9% sodium chloride 250 mL per bag' with the lot numbers 37-883926 through 37-898568 and expiration dates from May 2023 to June 2023.
Look for the lot numbers 37-883926 through 37-898568 and expiration dates from May 2023 to June 2023 on the product label.
An FDA inspection raised concerns about the sterility of these oxyTOCIN products, which are intended to be sterile but may not have been properly sterilized.
The lack of sterility could lead to infections if the product is used in medical procedures.
Check the product label for lot numbers 37-883926 through 37-898568 and expiration dates from May 2023 to 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-0708-2023 — Central Admixture Pharmacy Services Central Admixture Pharmacy Services Hello, I own a Central Admixture Pharmacy Services that is covered by recall D-0708-2023 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.
