SinuFrin Decongestant — Class III drug recall D-0569-2024
Ongoing recall by Neilmed Pharmaceuticals Inc, reported 2024-07-03, distributed nationwide. Sub-potent Drug
| Recall number | D-0569-2024 |
|---|---|
| Product type | Drug |
| Classification | Class III |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Neilmed Pharmaceuticals Inc, Santa Rosa, CA, United States |
| Recall initiated | 2024-06-24 |
| Classified | 2024-06-28 |
| Reported by FDA | 2024-07-03 |
| Distributed | Nationwide (US) |
| Quantity | 20,370 bottles |
| Reason classes | potency |
| UPC / GTIN / UDI-DI | 00705928090019 |
| NDC | 13709-0325, 13709-0325-01 |
| Lot numbers | SD134 |
| Expiration dates | 2026-10-31 |
Product
SinuFrin Decongestant (oxymetazoline HCl) Nasal Solution Nasal Decongestant, Decongestant Relief for up to 12 Hours, 12 Hour Relief, 0.5 fl oz (15 ml) bottle, Manufactured by NeilMed Pharmaceuticals Inc, 602 Aviation Blvd, Santa Rosa, CA 95403 877-477-8633; NDC 13709-325-01; UPC 7 05928 09001 9.
Reason for recall
Sub-potent Drug
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-0569-2024. 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.