United StatesPovidone Iodine 1.25% / Proparacaine HCl 0.5% Ophthalmic Solution, 10 mL per dropper bottle labeled “For Office Use Only” from Imprimis NJOF, LLC (NDC 71384-732-10) in lots 26JAN035 (BUD 09/07/2026) and 26FEB015 (BUD 09/24/2026) is affected; 772 bottles were distributed nationwide. The product is being recalled because it is subpotent. The recall is ongoing.
What's being recalled
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
Recalling firm: ImprimisRx NJ LLC, Ledgewood, NJ, United States.
How to identify it
Lot #: 26JAN035, BUD 09/07/2026; 26FEB015, BUD 09/24/2026
The hazard
Subpotent Drug
What to do
Don't stop taking a prescribed medicine without talking to your doctor or pharmacist first. For other products, stop using them and ask the pharmacist, seller or maker what to do.
The notice doesn't give instructions for consumers, so this is general advice for health & beauty recalls. Check the official notice for the details.
Where it was sold
USA Nationwide
The official notice
This page is a summary of the notice published by U.S. Food and Drug Administration (enforcement reports), collected from U.S. Food and Drug Administration (enforcement reports). Check the original before you act on it.
Read the official notice (opens in a new tab)