# FDA recall D-0029-2018

> **Becton Dickinson & Company** · Class II · drug recall initiated 2017-09-15.

## Product

ChloraPrep OneStep (Clear) (2% w/v chlorhexidine gluconate (CHG) and 70% v/v isopropyl alcohol (IPA)), 3 mL applicator, CareFusion, El Paso, TX 79912 --- NDC 054365-400-11

## Reason for recall

Labeling; Label Mixup; the immediate package is labeled incorrectly as Chloroprep Onestep (Clear), however, the correct label should be Chloroprep with Tint (Hi Lite Orange)

## Distribution

IL, MO, PA, TN, & VA

## Key facts

- **Recall number:** D-0029-2018
- **Recalling firm:** Becton Dickinson & Company
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2017-09-15
- **Report date:** 2017-11-01
- **Termination date:** 2018-06-27

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

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0029-2018

## Citation

> AI Analytics. FDA recall D-0029-2018. Retrieved 2026-06-03 from https://api.ai-analytics.org/recall/D-0029-2018. Source: US FDA. Licensed CC0.

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