Northern VA Compounders recalls TriMix Plus 001 injectable vials due to lack of sterility assurance. This compounded medication poses a risk of infection if used improperly.
Lack of Assurance of Sterility
Northern VA Compounders is recalling TriMix Plus 001 injectable vials because they may not be sterile. Using these vials could lead to infections, especially since they are compounded medications for medical use.
The vials may not be sterile, which can lead to infections if injected. This is particularly concerning for compounded medications used in medical treatments.
Patients prescribed this compounded medication by healthcare providers in the United States. Those using the vials for medical treatments are at risk of infection.
Check for vials labeled 'TriMix Plus 001 (PGE1/Papaverine HCl/Phentolamine Mesylate) 20mcg/30mg/2mg/mL INJECTABLE, 2.5 mL Multiple-Dose vials' compounded by Akina Pharmacy in Sterling, VA. Lot numbers 11252022@5 (expiring 1/9/2023) and 12012022@12 (expiring 1/15/2023) are affected.
Look for the product name and lot numbers listed in the recall notice to confirm if your vial is affected.
The recall states there is a lack of sterility assurance, so it is not safe to use without checking the recall status.
Check for vials labeled 'TriMix Plus 001 (PGE1/Papaverine HCl/Phentolamine Mesylate) 20mcg/30mg/2mg/mL INJECTABLE, 2.5 mL Multiple-Dose vials' compounded by Akina Pharmacy in Sterling, VA with lot numbers 11252022@5 or 12012022@12.
The recall does not specify a remedy, so contact your healthcare provider for guidance on safe disposal or alternative treatments.
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-0117-2023 — Northern VA Compounders Northern VA Compounders Hello, I own a Northern VA Compounders that is covered by recall D-0117-2023 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.
