FDA · Drugs ·
Povidone Iodine 1.25% / Proparacaine HCl 0.5% Ophthalmic Solution recall
ImprimisRx NJ LLC recalled Povidone Iodine 1.25% / Proparacaine HCl 0.5% Ophthalmic Solution on September 16, 2026 because of subpotent drug. It was sold nationwide.
Why it was recalled
Subpotent Drug
What's 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
Quantity: 772 bottles
What to do
Check whether you have the product (match the lot numbers, dates or codes in the official notice). Stop using it, and return it or throw it away as the notice says.
Read the official FDA noticeDetails
- Company
- ImprimisRx NJ LLC, Ledgewood, NJ
- Date
- Severity
- Class III
the product is unlikely to cause health problems but breaks a rule. - Where sold
- Nationwide
USA Nationwide - Status
- Ongoing
- Recall number
- D-0835-2026
- Source
- U.S. Food and Drug Administration
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