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 |
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.
How to identify the recalled item
| Lot / date codes | Lot AB6001, exp date 1/15/2027 |
|---|---|
| Lot / date codes | Lot AB6001, exp date 1/15/2027 |
These are the identifiers FDA published for this recall. Most recall notices list no UPC or model number at all — if the code on your item is not shown here, that does not mean the item is excluded. Check the official notice, or contact the company.
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.