# FDA recall D-0518-2026

> **CareFusion 213, LLC** · Class II · drug recall initiated 2026-04-22.

## Product

BD PurPrep, Povidone-iodine 8.3% w/w (0.83% available iodine) with isopropyl alcohol 72.5% w/w Sterile Solution, 0.36 fl. oz. (10.5 mL) x 25 applicators per box. Carefusion 213, LLC, El Paso, TX 79912, subsidary of Becton Dickinson and Co. NDC 54365-014-41

## Reason for recall

Lack of assurance of Sterility: potential product contamination

## Distribution

Nationwide in the USA

## Key facts

- **Recall number:** D-0518-2026
- **Recalling firm:** CareFusion 213, LLC
- **Classification:** Class II
- **Product type:** drug
- **Status:** Ongoing
- **Initiation date:** 2026-04-22
- **Report date:** 2026-05-13

- **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-0518-2026

## Citation

> AI Analytics. FDA recall D-0518-2026. Retrieved 2026-06-25 from https://api.ai-analytics.org/recall/D-0518-2026. Source: US FDA. Licensed CC0.

---

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