Central Admixture Pharmacy Services recalls oxyTOCIN 30 units added to Lactated Ringer's 500 mL IV bags due to lack of sterility assurance. These products were manufactured with validation data for decontamination cycles missing.
Lack of assurance of sterility. Validation data for decontamination cycles is lacking.
Central Admixture Pharmacy Services has recalled oxyTOCIN 30 units added to Lactated Ringer's 500 mL IV bags because the manufacturing process did not ensure sterility. This could lead to infections if the medication is used in medical settings.
The products lack validation data for decontamination cycles, meaning the sterility of the medication cannot be guaranteed. This could result in infections if the medication is administered to patients.
Healthcare professionals and patients receiving IV treatments with the recalled oxyTOCIN products. Those at highest risk are individuals undergoing medical procedures requiring sterile IV administration.
Check for the NDC code 72196-6039-1 or specific lot numbers listed in the recall notice. Products were sold with expiration dates from July 13, 2023, through August 11, 2023.
Identify the NDC code and lot numbers listed in the recall notice to confirm if your product is affected.
The recall is due to lack of validation data for decontamination cycles, which means the sterility of the medication cannot be assured.
The official recall notice does not specify a remedy, so contact Central Admixture Pharmacy Services for guidance.
Yes, the recall includes specific lot numbers with expiration dates from July 13, 2023, through August 11, 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-1012-2023 — Central Admixture Pharmacy Services Central Admixture Pharmacy Services Hello, I own a Central Admixture Pharmacy Services that is covered by recall D-1012-2023 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.
