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Home › FDA recalls › Albuterol Sulfate Inhalation Solution
CLASS II · ModerateFDA

Nephron SC, LLC recalls Albuterol Sulfate Inhalation Solution

📅 Mar 17, 2026 · 📍 Nationwide
Recalling company
Nephron SC, LLC
Product
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.
Reason
Labelling: Illegible label
Classification
Class II – may cause temporary or medically reversible health consequences
Recall date
Mar 17, 2026
Reported
Apr 22, 2026
Distribution
Nationwide within the United States
Status
Ongoing
Quantity
146,280 vials
Lot / codes
Lot AB6001, exp date 1/15/2027
Company location
West Columbia, SC
Recall type
Voluntary: Firm initiated
Recall number
D-0479-2026
Agency
U.S. Food and Drug Administration (FDA)

View official FDA notice ↗ Search recall number D-0479-2026 in the FDA Enforcement Report. Also see FDA recall press releases.

If you use this product, check the lot, NDC or model number against the official notice and follow its instructions. Do not stop a prescribed medicine or remove a medical device without talking to your doctor or pharmacist. Report problems to FDA MedWatch. FoodRecallNow summarizes public FDA data and is not medical advice.