Povidone Iodine 1 — Class III drug recall D-0835-2026
Ongoing recall by ImprimisRx NJ LLC, reported 2026-09-16, distributed nationwide. Subpotent Drug
| Recall number | D-0835-2026 |
|---|---|
| Product type | Drug |
| Classification | Class III |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | ImprimisRx NJ LLC, Ledgewood, NJ, United States |
| Recall initiated | 2026-08-24 |
| Classified | 2026-09-08 |
| Reported by FDA | 2026-09-16 |
| Distributed | Nationwide (US) |
| Quantity | 772 bottles |
| Reason classes | potency |
| NDC | 71384-0732-10 |
| Lot numbers | 26FEB015, 26JAN035 |
| Expiration dates | 2026-09-07, 2026-09-24 |
Product
Povidone Iodine 1.25% / Proparacaine HCl 0.5% Ophthalmic Solution, 10 mL per dropper bottle, For Office Use Only, Imprimis NJOF, LLC, 1705 Route 46 West, Unit 6B, Ledgewood, NJ 07852, NDC 71384-732-10
Reason for recall
Subpotent 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-0835-2026. 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.