ImprimisRx NJ LLC recalls Povidone Iodine 1.25% / Proparacaine HCl 0.5% Ophthalmic Solution
- Recalling company
- ImprimisRx NJ LLC
- Product
- 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
- Reason
- Subpotent Drug
- Classification
- Class III – not likely to cause adverse health consequences
- Recall date
- Aug 24, 2026
- Reported
- Sep 16, 2026
- Distribution
- USA Nationwide
- Status
- Ongoing
- Quantity
- 772 bottles
- Lot / codes
- Lot #: 26JAN035, BUD 09/07/2026; 26FEB015, BUD 09/24/2026
- Company location
- Ledgewood, NJ
- Recall type
- Voluntary: Firm initiated
- Recall number
- D-0835-2026
- Agency
- U.S. Food and Drug Administration (FDA)
View official FDA notice ↗ Search recall number D-0835-2026 in the FDA Enforcement Report. Also see FDA recall press releases.
If you use this product, check the lot, NDC or model number against the official notice and follow its instructions. Do not stop a prescribed medicine or remove a medical device without talking to your doctor or pharmacist. Report problems to FDA MedWatch. FoodRecallNow summarizes public FDA data and is not medical advice.