Nephron recalls albuterol inhaler vials with illegible labels. This may cause medication errors. Check your vial's label and NDC number for affected units.
Labelling: Illegible label
Nephron is recalling albuterol inhaler vials with illegible labels. This could lead to medication errors if users cannot properly identify the product.
Illegible labels make it difficult to identify the medication correctly. This could lead to using the wrong product or incorrect dosage, especially for people who rely on inhalers for breathing problems.
People who have the recalled albuterol inhaler vials with illegible labels. Those using the product for asthma or breathing issues are most at risk.
Check for vials with the label 'Albuterol Sulfate Inhalation Solution, 0.5%, 25 mg/5 mL (5 mg/mL*), 30x5 mL Sterile Unit-Dose Vials, Rx only'. The NDC number is 69374-330-05 and the lot number is AB6001.
Look for illegible labels on the vial. If the label is unreadable, stop using it.
The NDC number is 69374-330-05.
Check for vials with the label 'Albuterol Sulfate Inhalation Solution, 0.5%, 25 mg/5 mL (5 mg/mL*), 30x5 mL Sterile Unit-Dose Vials, Rx only' and NDC 69374-330-05.
The recall record does not mention a return or disposal requirement.
We’ve drafted a message you can send Nephron to request your refund or repair — edit it as you like.
Subject: Recall D-0479-2026 — Nephron Nephron Hello, I own a Nephron that is covered by recall D-0479-2026 from Nephron. 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.
