Albuterol Sulfate Inhalation Solution — Class II drug recall D-0479-2026
Ongoing recall by Nephron SC, LLC, reported 2026-04-22, distributed nationwide. Labelling: Illegible label
| Recall number | D-0479-2026 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Nephron SC, LLC, West Columbia, SC, United States |
| Recall initiated | 2026-03-17 |
| Classified | 2026-04-14 |
| Reported by FDA | 2026-04-22 |
| Distributed | Nationwide (US) |
| Quantity | 146,280 vials |
| Reason classes | labeling |
| NDC | 69374-0330-05 |
| Lot numbers | AB6001 |
| Expiration dates | 2027-01-15 |
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 for recall
Labelling: Illegible label
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/D-0479-2026. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.