Recalled oxyTOCIN 20 units added to Lactated Ringer's 1,000 mL bags due to potential sterility issues. Patients receiving these products may face infection risks.
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 has recalled oxyTOCIN 20 units added to Lactated Ringer's 1,000 mL bags because an FDA inspection raised concerns about sterility. This could lead to infections in patients receiving the product.
The FDA inspection found potential sterility issues in the products. If the product is not sterile, it could cause infections in patients who receive it through medical procedures.
Healthcare facilities and patients receiving oxyTOCIN 20 units added to Lactated Ringer's 1,000 mL bags. Patients with medical conditions requiring this medication are at risk of infection.
Check for the product name 'oxyTOCIN 20 units added to Lactated Ringer's 1,000 mL per bag' with the lot numbers listed in the recall notice. The products are labeled as 'Rx only' and manufactured by Central Admixture Pharmacy Services, Inc.
Identify the lot numbers and expiration dates listed in the recall notice to determine if your product is affected.
The FDA inspection raised concerns about sterility, so the product is not considered safe for use without recalling it.
Contact Central Admixture Pharmacy Services, Inc. to check if your product is affected and follow their instructions.
Check the lot numbers and expiration dates listed in the recall notice to see if they match the affected products.
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-0706-2023 — Central Admixture Pharmacy Services Central Admixture Pharmacy Services Hello, I own a Central Admixture Pharmacy Services that is covered by recall D-0706-2023 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.
