Class II โ€” Potential Health Hazard

Potential health hazard โ€” use of or exposure to this product may cause temporary or medically reversible adverse health consequences.

Timolol-Latanoprost (0.5/0.005%) ophthalmic drops Recalled by ImprimisRx NJ Due to Subpotent Drug: The batches contain less than 90%...

Date: November 9, 2022
Company: ImprimisRx NJ
Status: Terminated
Source: FDA (Drug)

What You Should Do

Stop using this product immediately. Do not consume, use, or distribute it.

Return the product to the place of purchase for a full refund. If you have questions, contact ImprimisRx NJ directly.

Affected Products

Timolol-Latanoprost (0.5/0.005%) ophthalmic drops, Compounded, 5 mL bottle, Imprimis Rx, Ledgewood, NJ.

Quantity: 960 bottles

Why Was This Recalled?

Subpotent Drug: The batches contain less than 90% of the labeled amount of latanoprost.

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

About ImprimisRx NJ

ImprimisRx NJ has 3 total recalls tracked by RecallDetector.

Related Recalls

Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report