Povidone Iodine 1 recall — ImprimisRx NJ LLC
Subpotent Drug
Company / brand: ImprimisRx NJ recalls
Affected product: Povidone Iodine 1 recall status
Official ID D-0835-2026 · Official record ↗
Notice names this product. ImprimisRx NJ’s Povidone Iodine 1 is named in FDA Class III recall D-0835-2026. Your particular item is not yet verified. Compare the identifiers and exclusions in the notice before deciding whether it applies. Agency-reported hazard: Subpotent Drug Identifying details: Lot #: 26JAN035, BUD 09/07/2026; 26FEB015, BUD 09/24/2026. Units affected: 772 bottles. Status: Ongoing.
This notice names a product; your particular item is not yet verified. Compare every applicable model, serial, lot, production-date or model-year boundary below.
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
Still to verify: match the label on your item with the full official notice, including any exclusions, tables and photos. Some identifiers appear only on the agency website and are absent from this data feed. A missing field does not mean all versions are affected.
If your lot or date falls outside a stated range, this notice has not established that your item is affected. This is not a finding about other recalls or product safety.
Subpotent Drug
Company / brand: ImprimisRx NJ recalls
Affected product: Povidone Iodine 1 recall status
Official ID D-0835-2026 · Official record ↗
See all ImprimisRx NJ recalls →
Found something wrong or missing? Report a data error.
Compiled from connected official public-domain government data. Sources last checked October 22, 2026 at 12:00 PM UTC.