Wells Pharma recalls fentanyl citrate injectable solution due to cGMP deviations. Affected lots: 022326203650432. Expired June 2026. No remedy specified in recall notice.
cGMP deviations.
Wells Pharma has recalled a specific fentanyl citrate injectable solution product due to manufacturing quality control issues. This recall is important because the product may not meet safety standards, potentially affecting patient safety during medical use.
The product was manufactured with cGMP (current Good Manufacturing Practice) deviations, which means it did not meet the required quality standards for safety and effectiveness. This could lead to inconsistent dosing or other safety issues during medical administration.
Healthcare professionals using this fentanyl solution for medical purposes are likely affected. Patients receiving this medication under medical supervision may also be at risk.
Check for the lot number 022326203650432 on the product label. The product expires June 25, 2026, and is labeled as fentanyl citrate injectable solution in 0.9% sodium chloride.
Look for the lot number 022326203650432 and expiration date of June 25, 2026 on the fentanyl citrate solution packaging.
The recall notice does not specify any remedy or action for consumers.
The product is fentanyl citrate injectable solution in 0.9% sodium chloride, 1000 mcg/50mL (20 mcg per mL), with lot number 022326203650432 and expiration date June 25, 2026.
The product was recalled due to cGMP deviations, which means it did not meet the required quality standards for safety and effectiveness.
We’ve drafted a message you can send Wells Pharma to request your refund or repair — edit it as you like.
Subject: Recall D-0506-2026 — Wells Pharma Wells Pharma Hello, I own a Wells Pharma that is covered by recall D-0506-2026 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
