ImprimisRx NJ recalls ophthalmic solution for subpotency, Class III
The FDA lists a Class III recall of 772 bottles of a povidone iodine and proparacaine ophthalmic solution made by ImprimisRx NJ LLC.
The only item this week is a drug recall enforcement record.
- ImprimisRx NJ LLC initiated a voluntary recall of Povidone Iodine 1.25% / Proparacaine HCl 0.5% Ophthalmic Solution, sold in 10 mL dropper bottles for office use only under NDC 71384-732-10, citing the reason "Subpotent Drug."1 The recall covers 772 bottles distributed nationwide across the USA1, was initiated on 202608241, and is classified as Class III1 with a status of Ongoing1 as of the report date of 202609161.
Written by readthrough’s AI from the linked primary sources and fact-checked against them automatically before publishing. Not investment advice.