Central Admixture Pharmacy Services recalls oxyTOCIN 15 units in IV bags due to lack of sterility assurance. Affected lots expire through September 2023. Consumers should contact the manufacturer for details.
Lack of assurance of sterility. Validation data for decontamination cycles is lacking.
Central Admixture Pharmacy Services is recalling oxyTOCIN 15 units added to 0.9% sodium chloride IV bags because the product lacks proper sterility assurance. This could lead to infections if the medication is used without being sterile.
The product lacks validation data for decontamination cycles, meaning it may not be sterile. If the medication is not sterile, it could cause infections when administered to patients.
Patients receiving oxyTOCIN 15 units via IV infusion from the recalled lots. Healthcare providers using these specific IV bags for medical treatments are at risk.
Check the product label for the NDC code 72196-6042-1 and lot numbers listed in the recall (e.g., 36-241662 through 36-254917). The expiration dates range from July 2023 to September 2023.
Look for the NDC code 72196-6042-1 and lot numbers listed in the recall (e.g., 36-241662 through 36-254917).
oxyTOCIN 15 units added to 0.9% sodium chloride 250 mL IV bags, NDC 72196-6042-1, with specific lot numbers listed in the recall.
Check the product label for the NDC code 72196-6042-1 and lot numbers from 36-241662 through 36-254917, which expire through September 2023.
The recall does not specify a remedy, so contact Central Admixture Pharmacy Services for further instructions.
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-0973-2023 — Central Admixture Pharmacy Services Central Admixture Pharmacy Services Hello, I own a Central Admixture Pharmacy Services that is covered by recall D-0973-2023 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.
