QuVa Pharma recalls specific lots of Methohexital Sodium compounded drug due to failed impurities and degradation specifications. This recall affects certain prescription-only products sold in Texas.
Failed Impurities/Degradation Specifications
QuVa Pharma is recalling specific lots of Methohexital Sodium compounded drug because it failed impurities and degradation specifications. This means the product could be unsafe for medical use, though the exact risk isn't detailed in the recall notice.
The product failed impurities and degradation specifications, which means it may contain harmful substances or break down in a way that could affect safety during medical use. However, the recall does not specify the exact risk or how it could cause harm.
Prescription-only Methohexital Sodium compounded drugs manufactured by QuVa Pharma in Sugar Land, Texas. Healthcare providers who dispensed the recalled lots are most at risk.
Check for the product code 70092-1310-46 on the label. The recall includes specific lot numbers and expiration dates from July 2026 through August 2026.
Look for the product code 70092-1310-46 and the listed lot numbers on the label.
The recall states the product failed impurities and degradation specifications, but does not specify if it is safe to use. Do not use the product until you confirm it is not recalled.
The recall does not provide a remedy, so contact QuVa Pharma directly for guidance on what to do with the product.
Check the product code 70092-1310-46 and the listed lot numbers on the label to see if it matches the recalled items.
We’ve drafted a message you can send QuVa Pharma to request your refund or repair — edit it as you like.
Subject: Recall D-0664-2026 — QuVa Pharma QuVa Pharma Hello, I own a QuVa Pharma that is covered by recall D-0664-2026 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.
