FDA · Drugs ·
Albuterol Sulfate Inhalation Solution recall
Nephron SC, LLC recalled Albuterol Sulfate Inhalation Solution on April 22, 2026 because of labelling: Illegible label. It was sold nationwide.
Why it was recalled
Labelling: Illegible label
What's recalled
Albuterol Sulfate Inhalation Solution, 0.5%, 25 mg/5 mL (5 mg/mL*), 30x5 mL Sterile Unit-Dose Vials, Rx only, nephron 503B Outsourcing facility, 4600 12th Street Extension, West Columbia, SC 29172, NDC 69374-330-05.
Quantity: 146,280 vials
What to do
Check whether you have the product (match the lot numbers, dates or codes in the official notice). Stop using it, and return it or throw it away as the notice says.
Read the official FDA noticeDetails
- Company
- Nephron SC, LLC, West Columbia, SC
- Date
- Severity
- Class II
the product could cause temporary or reversible health problems. - Where sold
- Nationwide
Nationwide within the United States - Status
- Ongoing
- Recall number
- D-0479-2026
- Source
- U.S. Food and Drug Administration
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