Class II · ModerateActive recall
Albuterol Sulfate Inhalation Solution
Could cause temporary or reversible harm; serious harm is unlikely.
Does this affect you?
Check your lot numberLot AB6001, exp date 1/15/2027
Where it was soldNationwide within the United States
Find the lot number printed on your box or bottle. If it matches — and you take this medicine — call your pharmacist. Don't stop a prescribed medicine on your own.
What happened
Labelling: Illegible label
What to do
- Check the lot number and expiry on your medicine against the recall above.
- Talk to your pharmacist or doctor before changing anything — don't stop on your own.
- Report any problems to FDA MedWatch (1-800-FDA-1088 or fda.gov/medwatch).
Who makes it
| Distributed by / for | Nephron SC, LLC |
| NDC | 69374-330-05 |
Show the full FDA record
| Full product label | 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. |
| Recalling firm | Nephron SC, LLC |
| Distribution | Nationwide within the United States |
| Quantity | 146,280 vials |
| Recall initiated | 2026-03-17 |
| Report date | 2026-04-22 |
| Recall completed | — |
| Recall number | D-0479-2026 |
| Classification | Class II |
| FDA status | Ongoing |
| Origin on file | West Columbia SC United States |
Source: U.S. FDA enforcement database (openFDA). Look this up on the official FDA recalls site ↗
This is public FDA recall information, not medical advice. A recall does not always mean your specific bottle is affected. Never stop a prescribed medicine without asking your pharmacist or doctor.