Wells Pharma recalls fentanyl injectable solution (NDC 73702-204-25) manufactured with cGMP deviations. Affected lots may pose quality risks.
cGMP deviations.
Wells Pharma is recalling fentanyl injectable solution due to manufacturing deviations. This could affect product quality and safety for patients using the medication.
The product was manufactured with cGMP deviations, which are quality control failures in drug production. This could lead to inconsistent drug strength or safety issues.
Patients using this fentanyl injectable solution are affected. Healthcare providers administering the medication may also be at risk.
Check for the NDC number 73702-204-25 on the label. The lot number 011226204250063 and expiration date 05/14/2026 are also specific identifiers.
Look for the NDC number 73702-204-25 and lot number 011226204250063 on the label.
The recall states manufacturing deviations occurred, but does not specify if the product is safe to use. The official notice does not provide details on whether the product poses a risk.
The recall does not specify any remedy or action steps for affected products. The official notice does not provide instructions on what to do with the product.
Check the label for NDC 73702-204-25 and lot number 011226204250063. The expiration date is 05/14/2026.
We’ve drafted a message you can send Wells Pharma to request your refund or repair — edit it as you like.
Subject: Recall D-0505-2026 — Wells Pharma Wells Pharma Hello, I own a Wells Pharma that is covered by recall D-0505-2026 from Wells 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.
