Central Admixture Pharmacy Services recalls oxyTOCIN 30 units in 0.9% sodium chloride IV bags due to lack of sterility assurance. Products with specific NDC and lot numbers listed in the recall are affected.
Lack of assurance of sterility. Validation data for decontamination cycles is lacking.
Central Admixture Pharmacy Services has recalled oxyTOCIN 30 units added to 0.9% sodium chloride IV bags because of a lack of sterility assurance. This means the product could be contaminated, posing a risk of infection if used.
The product lacks validation data for decontamination cycles, which means it may not be sterile. This could lead to infections if the medication is administered.
Healthcare professionals and patients who have received the recalled oxyTOCIN IV bags. Those using the product for medical treatments are most at risk.
Check for the NDC code 72196-6044-1 and lot numbers listed in the recall (e.g., 36-238820 to 36-255615) on the packaging. The products were sold with expiration dates from July 10, 2023, to September 7, 2023.
Look for the NDC code 72196-6044-1 and lot numbers listed in the recall on the packaging.
The product has been recalled due to a lack of sterility assurance, so it is not safe to use. It could lead to infections if administered.
Check the product details against the list of recalled items. If it matches, stop using it and contact your healthcare provider.
Look for the NDC code 72196-6044-1 and lot numbers listed in the recall (e.g., 36-238820 to 36-255615) on the packaging.
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-0986-2023 — Central Admixture Pharmacy Services Central Admixture Pharmacy Services Hello, I own a Central Admixture Pharmacy Services that is covered by recall D-0986-2023 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.
