Northern VA Compounders recalls QuadMix Injectable (PGE1/Papaverine HCl/Phentolamine Mesylate/Atropine) 20mcg/20mg/2mg/0.2mg/mL 2.5mL vials due to lack of sterility assurance. Rx only, compounded by Akina Pharmacy in Sterling, VA. No remedy specified.
Lack of Assurance of Sterility
Northern VA Compounders is recalling QuadMix Injectable vials because they lack assurance of sterility. This means the medication could be contaminated, posing a risk of infection or illness if used.
The vials lack assurance of sterility, meaning they could be contaminated with bacteria or other pathogens. If injected, this could lead to serious infections or health complications.
Patients prescribed this compounded medication by a healthcare provider in the United States. Those using the product without medical supervision are not affected.
Look for QuadMix Injectable vials labeled 20mcg/20mg/2mg/0.2mg/mL in 2.5 mL size. They were compounded by Akina Pharmacy in Sterling, VA and have lot number 11292022@12 with an expiration date of January 13, 2023.
Verify the product label matches the described QuadMix Injectable vials with lot number 11292022@12 and expiration date 1/13/2023.
The recall states there is a lack of assurance of sterility, so the product is not safe to use as it could be contaminated.
Look for QuadMix Injectable vials labeled 20mcg/20mg/2mg/0.2mg/mL in 2.5 mL size, compounded by Akina Pharmacy in Sterling, VA with lot number 11292022@12 and expiration date 1/13/2023.
The recall does not specify a remedy, so contact your healthcare provider for guidance on safe handling or disposal.
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-0120-2023 — Northern VA Compounders Northern VA Compounders Hello, I own a Northern VA Compounders that is covered by recall D-0120-2023 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.
