# FDA recall D-0516-2024

> **Imprimis NJOF, LLC** · Class II · drug recall initiated 2024-05-14.

## Product

Moxifloxacin 4 mg/0.8 mL Preservative-Free 0.8mL Single-Use vials for Intraocular Injection, Rx only, Imprimis NJOF, LLC. 1705 Route 46 West, unit 6B, Ledgewood, NJ 07852, NDC 71384-511-08

## Reason for recall

Lack of Assurance of Sterility

## Distribution

Nationwide within the United States

## Key facts

- **Recall number:** D-0516-2024
- **Recalling firm:** Imprimis NJOF, LLC
- **Classification:** Class II
- **Product type:** drug
- **Status:** Ongoing
- **Initiation date:** 2024-05-14
- **Report date:** 2024-06-05

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Ledgewood, NJ, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0516-2024

## Citation

> AI Analytics. FDA recall D-0516-2024. Retrieved 2026-07-06 from https://api.ai-analytics.org/recall/D-0516-2024. Source: US FDA. Licensed CC0.

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*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*