Wells Pharma recalls fentanyl citrate injectable solution due to cGMP deviations. Affected lots: NDC 73702-202-15, Lot 020226202150202. Expired May 2026.
cGMP deviations.
Wells Pharma is recalling fentanyl citrate injectable solution because of manufacturing quality control issues. This affects specific lots that may have safety risks if used improperly.
The recall is due to cGMP deviations, which means the product may not meet the strict quality standards required for safe medical use. This could potentially lead to incorrect dosing or other safety issues if the medication is not manufactured properly.
Healthcare professionals using the fentanyl citrate injectable solution for medical purposes. Patients receiving this medication under medical supervision.
Check for the NDC number 73702-202-15 and lot number 020226202150202 on the product label. The expiration date is May 5, 2026.
Look for the NDC number 73702-202-15 and lot number 020226202150202 on the product label.
The recall is due to cGMP deviations, which means the product may not meet quality standards. It is not safe to use without following the recall instructions.
The recall does not specify a remedy, so contact Wells Pharma directly for guidance.
The lot number 020226202150202 indicates the product was manufactured in 2022.
We’ve drafted a message you can send Wells Pharma to request your refund or repair — edit it as you like.
Subject: Recall D-0508-2026 — Wells Pharma Wells Pharma Hello, I own a Wells Pharma that is covered by recall D-0508-2026 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.