Central Admixture Pharmacy Services recalls oxyTOCIN 10 units added to Lactated Ringer's 500 mL IV bags due to lack of sterility assurance. Products with specific NDC and lot numbers are affected.
Lack of assurance of sterility. Validation data for decontamination cycles is lacking.
Central Admixture Pharmacy Services is recalling oxyTOCIN 10 units added to Lactated Ringer's 500 mL IV bags because the manufacturing process may not ensure sterility. This could lead to infections if the product is used in medical treatments.
The recall states that validation data for decontamination cycles is lacking, meaning the product may not be sterile. If the product is used in medical treatments, it could cause infections in patients.
Healthcare professionals and patients receiving IV treatments with the recalled oxyTOCIN products. Those using the specific lot numbers and expiration dates listed are most at risk.
Check for the NDC number 72196-6036-1 and specific lot numbers: 36-246733, 36-247777, 36-247779, 36-250334, 36-251383, 36-251384, 36-251990. Products with expiration dates from July 2023 through August 2023 are affected.
Identify the NDC number and lot numbers listed in the recall notice to confirm if your product is affected.
The recall states that validation data for decontamination cycles is lacking, so the product may not be sterile. Do not use the affected products.
The recall does not specify a remedy, so contact Central Admixture Pharmacy Services for guidance.
Check for the NDC number 72196-6036-1 and specific lot numbers: 36-246733, 36-247777, 36-247779, 36-250334, 36-251383, 36-251384, 36-251990.
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-0972-2023 — Central Admixture Pharmacy Services Central Admixture Pharmacy Services Hello, I own a Central Admixture Pharmacy Services that is covered by recall D-0972-2023 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.
