# FDA recall D-0992-2015

> **Cody Laboratories, Inc.** · Class II · drug recall initiated 2015-03-31.

## Product

C-Topical 4% CII (cocaine hydrochloride), topical solution, 4 ml bottle, (NDC 0527-1728-74), Rx Only, Manufactured for Lannett Company, Inc. Philadelphia, PA 19136 by Cody Laboratories, Inc. Cody, WY 82414

## Reason for recall

Labeling: Label mix-up; bottles were incorrectly labeled as 10 mL instead of correctly labeled as 4 mL

## Distribution

Nationwide

## Key facts

- **Recall number:** D-0992-2015
- **Recalling firm:** Cody Laboratories, Inc.
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2015-03-31
- **Report date:** 2015-05-13
- **Termination date:** 2015-10-14

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Cody, WY, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0992-2015

## Citation

> AI Analytics. FDA recall D-0992-2015. Retrieved 2026-05-25 from https://api.ai-analytics.org/recall/D-0992-2015. Source: US FDA. Licensed CC0.

---

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