US Drug Recall Register
Class II · Moderate risk Terminated Initiated Nov 29, 2021 (5 years ago)

Moxifloxacin, 1 mg/mL, 1mL in 2mL vial, solution for intracameral injection, 10…

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

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

What was recalled

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

Recalling firm
Denver Solutions, LLC DBA Leiters Health
NDC code
71449-096-42
Origin
CO, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0288-2022

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.

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