Class III · Lower riskActive recall
Povidone Iodine 1.25% / Proparacaine HCl 0.5% Ophthalmic Solution
Unlikely to cause harm — often a labeling or packaging issue.
Does this affect you?
Check your lot numberLot #: 26JAN035, BUD 09/07/2026; 26FEB015, BUD 09/24/2026
Where it was soldUSA Nationwide
Find the lot number printed on your box or bottle. If it matches — and you take this medicine — call your pharmacist. Don't stop a prescribed medicine on your own.
What happened
Subpotent Drug
What to do
- Check the lot number and expiry on your medicine against the recall above.
- Talk to your pharmacist or doctor before changing anything — don't stop on your own.
- Report any problems to FDA MedWatch (1-800-FDA-1088 or fda.gov/medwatch).
Who makes it
| Distributed by / for | ImprimisRx NJ LLC |
| NDC | 71384-732-10 |
Show the full FDA record
| Full product label | 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 |
| Distribution | USA Nationwide |
| Quantity | 772 bottles |
| Recall initiated | 2026-08-24 |
| Report date | 2026-09-16 |
| Recall completed | — |
| Recall number | D-0835-2026 |
| Classification | Class III |
| FDA status | Ongoing |
| Origin on file | Ledgewood NJ United States |
Source: U.S. FDA enforcement database (openFDA). Look this up on the official FDA recalls site ↗
This is public FDA recall information, not medical advice. A recall does not always mean your specific bottle is affected. Never stop a prescribed medicine without asking your pharmacist or doctor.