Fresh Recalls

Povidone Iodine 1: recall status

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.

1. Compare your item

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.

Product named
Povidone Iodine 1
Company / brand
ImprimisRx NJ
Lot / serial / date codes
Lot #: 26JAN035, BUD 09/07/2026; 26FEB015, BUD 09/24/2026
Distribution
USA Nationwide
Agency product description and boundaries

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.

Brand
ImprimisRx NJ

Recalls naming this model

FDA Class III · Drug · September 16, 2026

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 ↗

See all ImprimisRx NJ recalls →

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Compiled from connected official public-domain government data. Sources last checked October 22, 2026 at 12:00 PM UTC.