Central Admixture Pharmacy Services recalls oxyTOCIN 60 units added to 0.9% sodium chloride 1,000 mL bags due to potential contamination after FDA inspection. Affected lots expire April 2023 through June 2023.
Lack of Assurance of Sterility: after an FDA inspection called into question the sterility of the products intended to be sterile.
Central Admixture Pharmacy Services is recalling oxyTOCIN 60 units added to 0.9% sodium chloride 1,000 mL bags because an FDA inspection raised concerns about sterility. This could lead to infections if the product is used in medical treatments.
The FDA inspection found potential contamination in the sterile products. If the oxyTOCIN solution is not properly sterile, it could cause infections when used in medical procedures.
Healthcare professionals using these oxyTOCIN bags for medical treatments. Patients receiving the medication through these bags are at risk if the product is contaminated.
Look for bags labeled 'oxyTOCIN 60 units added to 0.9% sodium chloride 1,000 mL per bag, Rx only' with lot numbers 37-883073 through 37-898552 and expiration dates from April 2023 to June 2023.
Identify the lot number on the bag, which should be one of 37-883073, 37-887776, 37-889209, 37-892588, 37-894449, or 37-898552.
The FDA inspection raised concerns about sterility, so the product may not be safe for medical use. Do not use these bags until the recall is resolved.
Check the lot number on the bag. If it matches the affected lots listed, stop using it and contact Central Admixture Pharmacy Services for further instructions.
The recall record does not specify a replacement process. Contact Central Admixture Pharmacy Services directly for assistance.
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-0711-2023 — Central Admixture Pharmacy Services Central Admixture Pharmacy Services Hello, I own a Central Admixture Pharmacy Services that is covered by recall D-0711-2023 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.
