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.

Moxifloxacin Recalled by Denver Solutions, LLC DBA Leiters Health Due to Labeling: Label Mix-up: Vials labeled as moxifloxacin 1...

Date: November 29, 2021
Company: Denver Solutions, LLC DBA Leiters Health
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 Denver Solutions, LLC DBA Leiters Health directly.

Affected Products

Moxifloxacin, 1 mg/mL, 1mL in 2mL vial, solution for intracameral injection, 10 vials/carton, Rx only, Leiters 13796 Compark Blvd, Englewood, CO 80112, (800) 292-6772, NDC 71449-096-42

Quantity: 1440 vials

Why Was This Recalled?

Labeling: Label Mix-up: Vials labeled as moxifloxacin 1 mg/mL may actually contain moxifloxacin 5 mg/mL

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

About Denver Solutions, LLC DBA Leiters Health

Denver Solutions, LLC DBA Leiters Health has 22 total recalls tracked by RecallDetector.

Related Recalls

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