FDA Class III · Drug · September 16, 2026
Povidone Iodine 1 recall — ImprimisRx NJ LLC
Subpotent Drug
Official ID D-0835-2026 · Official record ↗
Recall found. ImprimisRx NJ is named in FDA Class III recall D-0835-2026 covering Povidone Iodine 1. Hazard: Subpotent Drug Identifying details: Lot #: 26JAN035, BUD 09/07/2026; 26FEB015, BUD 09/24/2026. Status: Ongoing.
Subpotent Drug
Official ID D-0835-2026 · Official record ↗
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Compiled from official public-domain government data. Last checked October 22, 2026 at 12:00 PM UTC.