# FDA recall D-0661-2017

> **Akorn, Inc.** · Class II · drug recall initiated 2017-03-17.

## Product

LATANOPROST OPHTHALMIC SOLUTION, 0.005%,  125 ug/2.5 mL, packaged in 2.5 mL bottle, Rx only,  Manufactured for: Akorn, Inc., Lake Forest, IL 60045, NDC 17478-625-12

## Reason for recall

Lack of assurance of sterility: product was found to be empty, under-filled, or leaking.

## Distribution

Nationwide

## Key facts

- **Recall number:** D-0661-2017
- **Recalling firm:** Akorn, Inc.
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2017-03-17
- **Report date:** 2017-04-19
- **Termination date:** 2019-07-09

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Lake Forest, IL, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0661-2017

## Citation

> AI Analytics. FDA recall D-0661-2017. Retrieved 2026-06-02 from https://api.ai-analytics.org/recall/D-0661-2017. Source: US FDA. Licensed CC0.

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