# FDA recall D-0288-2022

> **Denver Solutions, LLC DBA Leiters Health** · Class II · drug recall initiated 2021-11-29.

## Product

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

## Reason for recall

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

## Distribution

Nationwide within the United States

## Key facts

- **Recall number:** D-0288-2022
- **Recalling firm:** Denver Solutions, LLC DBA Leiters Health
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2021-11-29
- **Report date:** 2021-12-29
- **Termination date:** 2022-07-12

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Englewood, CO, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0288-2022

## Citation

> AI Analytics. FDA recall D-0288-2022. Retrieved 2026-07-15 from https://api.ai-analytics.org/recall/D-0288-2022. Source: US FDA. Licensed CC0.

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