Northern VA Compounders recalls QuadMix Super 002 injectable medication due to lack of sterility assurance. This compounded drug may cause infections if used improperly. Affected lots were sold in Virginia starting June 2022.
Lack of Assurance of Sterility
Northern VA Compounders has recalled a compounded injectable medication called QuadMix Super 002 because it lacks sterility assurance. This means the product could cause infections if used, especially in medical settings where sterile injections are critical.
The medication was compounded without proper sterility checks, meaning it could contain harmful bacteria or other contaminants. If injected, this could lead to serious infections, especially in vulnerable patients or during medical procedures.
Healthcare professionals and patients prescribed this compounded medication in Virginia starting June 2022. Those using the product for medical treatments are most at risk of infection.
Check for the product name 'QuadMix Super 002' with the lot number 12062022@1, packaged in 2.5 mL vials. It was sold in Virginia starting June 2022 and requires a prescription.
Look for the lot number 12062022@1 on the vial label to confirm if it's affected.
The official recall states there is a lack of sterility assurance, so it is not safe to use.
Check for the lot number 12062022@1 on the vial label and confirm it was sold in Virginia starting June 2022.
The recall does not specify a remedy, so contact Northern VA Compounders for guidance.
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-0108-2023 — Northern VA Compounders Northern VA Compounders Hello, I own a Northern VA Compounders that is covered by recall D-0108-2023 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.