Albuterol Recall: AB6001 Lot
Announced 2026-04-22 · FDA
FDA recalls 146,280 vials of Albuterol Sulfate Inhalation Solution due to illegible label. The recall is nationwide within the United States and involves Lot AB6001 with expiration date 1/15/2027.
| Brand | 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 |
| Severity | moderate |
| Units affected | 146280 |
| Distribution | Nationwide within the United States |
| Agency | FDA |
| Recall / campaign no. | Lot AB6001, exp date 1/15/2027 |
WHAT YOU SHOULD DO
- Do not use any product that bears Lot AB6001.
- Contact your healthcare provider or pharmacist for guidance and possible replacement.
- Return or dispose of the product according to local guidelines.
- If you experience an adverse event, report it to FDA MedWatch.
This is an automatically maintained record of an official recall notice. Details can change; always follow the official notice linked above. See all records in the Recall Database.