QuVa Pharma recalls fentanyl and bupivacaine solution for epidural use due to lack of sterility assurance. This compounded product may cause infections if used improperly. Check NDC 70092-1255-75 and lots 10140259-10140688.
Lack of Assurance of Sterility
QuVa Pharma has recalled a compounded epidural injection solution because it lacks sterility assurance. This means the product could cause infections if used in medical procedures. Patients and healthcare providers should stop using this specific product and contact the manufacturer for details.
The solution was compounded without proper sterility assurance, meaning it could be contaminated with bacteria. If used in epidural procedures, this contamination could lead to infections at the injection site.
Healthcare providers and patients using this compounded epidural solution for medical procedures. Those with the specific NDC and lot numbers are most at risk.
Check for the NDC number 70092-1255-75 and lot numbers 10140259, 10140539, 10140687, or 10140688 on the product label. The product is labeled for epidural use only, not for IV use.
Look for the NDC number 70092-1255-75 and lot numbers 10140259-10140688 on the product label.
No, this product has been recalled due to lack of sterility assurance, which could lead to infections if used in epidural procedures.
Check the product label for the NDC number 70092-1255-75 and lot numbers 10140259-10140688. If you have these, stop using it and contact QuVa Pharma for instructions.
No, this product has been recalled and should not be used for epidural procedures due to the risk of infection.
We’ve drafted a message you can send QuVa Pharma to request your refund or repair — edit it as you like.
Subject: Recall D-0295-2025 — QuVa Pharma QuVa Pharma Hello, I own a QuVa Pharma that is covered by recall D-0295-2025 from QuVa Pharma. 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.
