# FDA recall Z-0909-2025

> **Cardinal Health 200, LLC** · Class II · device recall initiated 2024-11-08.

## Product

Cardinal Health Presource Kits:  1 )	TRIPLE ENDO PACK, Catalog Number: SBAOCTEHH1:;  2 )	TRIPLE ENDO PACK, Catalog Number: SBAOCTEHHA:;  3 )	RIVERSIDE SINUS ENDOSCOPY PK, Catalog Number: SEN15SERM5:;  4 )	RIVERSIDE SINUS ENDOSCOPY PK, Catalog Number: SEN15SERMO:;  5 )	RIVERSIDE SINUS ENDOSCOPY PK, Catalog Number: SEN15SERMP:;

## Reason for recall

Potential endotoxin contamination in non-sterile surgical strips and patties in Presource kits.

## Distribution

Worldwide distribution - US Nationwide and the countries of Canada, Saudi Arabia.

## Key facts

- **Recall number:** Z-0909-2025
- **Recalling firm:** Cardinal Health 200, LLC
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2024-11-08
- **Report date:** 2025-01-22

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

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0909-2025

## Citation

> AI Analytics. FDA recall Z-0909-2025. Retrieved 2026-08-11 from https://api.ai-analytics.org/recall/Z-0909-2025. Source: US FDA. Licensed CC0.

---

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