Northern VA Compounders recalls QuadMix Standard 002 injectable due to lack of sterility assurance. This compounded medication may cause infections if used.
Lack of Assurance of Sterility
Northern VA Compounders is recalling QuadMix Standard 002 injectable medication because it lacks sterility assurance. This could lead to infections if the product is used.
The medication was compounded without proper sterility testing, which means it could contain harmful bacteria or other contaminants. If injected, this could cause serious infections or other health issues.
Prescription users of this compounded injectable medication in the United States. Patients receiving this specific medication from Akina Pharmacy in Sterling, VA are most at risk.
Look for the QuadMix Standard 002 injectable in 2.5 mL vials, labeled with lot number 12012022@11, and expired by January 15, 2023. This product was compounded by Akina Pharmacy in Sterling, VA.
Verify the lot number and expiration date on the vial to confirm if it matches the recalled batch.
The recall states there is a lack of sterility assurance, so it is not safe to use. The product may cause infections if injected.
The recall record does not specify a replacement process or remedy.
This medication was compounded by Akina Pharmacy in Sterling, VA.
We’ve drafted a message you can send Northern VA Compounders to request your refund or repair — edit it as you like.
Subject: Recall D-0104-2023 — Northern VA Compounders Northern VA Compounders Hello, I own a Northern VA Compounders that is covered by recall D-0104-2023 from Northern VA Compounders. 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.
