# FDA recall D-1510-2020

> **CareFusion 213, LLC** · Class I · drug recall initiated 2020-06-23.

## Product

ChloraPrep With Tint (2% w/v chlorhexidine gluconate (CHG) and 70% v/v isopropyl alcohol (IPA)) 3 mL applicators - Hi-Lite Orange  25 applicators in carton, CareFusion El Paso, TX 79912, subsidiary of Becton, Dickinson and Company, NDC 054365-400-11

## Reason for recall

Non-Sterility: Product is being recalled due to presence of Aspergillus Penicilloides

## Distribution

Puerto Rico, Guam, United Arab Emirates, Bahrain, Brazil, Democratic Republic of the Congo, Chile, Colombia, United Kingdom of Great Britain and Northern Ireland, Hong Kong, Israel, Kuwait, Oman, Qatar, Saudi Arabia, Singapore,

## Key facts

- **Recall number:** D-1510-2020
- **Recalling firm:** CareFusion 213, LLC
- **Classification:** Class I
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2020-06-23
- **Report date:** 2020-08-26
- **Termination date:** 2022-09-28

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** El Paso, TX, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-1510-2020

## Citation

> AI Analytics. FDA recall D-1510-2020. Retrieved 2026-06-25 from https://api.ai-analytics.org/recall/D-1510-2020. Source: US FDA. Licensed CC0.

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