FDA Drug · D-0835-2026

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

Class III · Ongoing

Subpotent Drug

Affected lots / codes — check yours against thisLot #: 26JAN035, BUD 09/07/2026; 26FEB015, BUD 09/24/2026

Recalling firm: ImprimisRx NJ LLC, Ledgewood, NJ
Classification: Class III (unlikely to cause harm)
Status: Ongoing
Quantity: 772 bottles
Distribution: USA Nationwide
Recall initiated: August 24, 2026
Classified: September 8, 2026
Initiation: Voluntary: Firm initiated

Official source. This record is published by the U.S. FDA through the openFDA enforcement database. View the unmodified government record:
https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0835-2026%22

Important. Recalls target specific lots and codes — compare the affected lots above against your own product. This page reproduces public FDA data for readability; EveryRecall is independent and not affiliated with the FDA.

Check this brand across all 8 databases →