Central Admixture Pharmacy Services recalls oxyTOCIN 20 units added to 0.9% saline for medical use due to potential lack of sterility after FDA inspection. This may cause infections if used improperly.
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 20 units added to 0.9% sodium chloride (saline) for medical use because an FDA inspection raised concerns about the products' sterility. Using these products could lead to infections if they are not 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 solution is used in medical procedures without being sterile.
Healthcare professionals and patients who have received this specific oxyTOCIN saline solution from Central Admixture Pharmacy Services. Those using it for medical purposes are most at risk.
Check for the product name 'oxyTOCIN 20 units added to 0.9% sodium chloride 1,000 mL per bag' with the manufacturer Central Admixture Pharmacy Services. Look for lot numbers listed in the recall notice (e.g., 37-883938) and expiration dates (e.g., 05/02/2023).
Identify the product by checking the lot number and expiration date on the packaging.
The FDA inspection raised concerns about sterility, so these products may not be safe for medical use. Do not use until the recall is addressed.
Contact Central Admixture Pharmacy Services for guidance on how to handle the recalled product.
Check the lot number and expiration date on the packaging against the list provided in the recall notice.
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-0709-2023 — Central Admixture Pharmacy Services Central Admixture Pharmacy Services Hello, I own a Central Admixture Pharmacy Services that is covered by recall D-0709-2023 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.
