Central Admixture Pharmacy Services recalls oxyTOCIN 20 units IV bags due to lack of sterility assurance. These products may cause infections if used without proper sterilization.
Lack of assurance of sterility. Validation data for decontamination cycles is lacking.
Central Admixture Pharmacy Services is recalling oxyTOCIN 20 units IV bags that were added to 0.9% sodium chloride. The recall is due to a lack of assurance of sterility, which could lead to infections if the product is used without proper sterilization.
The IV bags lack validation data for decontamination cycles, meaning they may not be sterile when prepared. This could lead to infections if the product is used without proper sterilization procedures.
Healthcare professionals who use these IV bags for medical treatments may be affected. Patients receiving oxyTOCIN treatments through these bags are at risk of infection.
Check for the product name 'oxyTOCIN 20 units added to 0.9% sodium chloride 1,000 mL, IV Bag' with the manufacturer Central Admixture Pharmacy Services. Look for specific lot numbers and expiration dates listed in the recall notice.
Identify the lot number and expiration date on the IV bag to determine if it is part of the recall.
The recall states there is a lack of assurance of sterility, so these products should not be used until the recall is resolved.
The recall does not specify a remedy, so contact the manufacturer for guidance on safe disposal or alternatives.
Check the lot number and expiration date 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-0976-2023 — Central Admixture Pharmacy Services Central Admixture Pharmacy Services Hello, I own a Central Admixture Pharmacy Services that is covered by recall D-0976-2023 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.
