# FDA recall Z-1130-2025

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

## Product

Cardinal Health Presource Kits:  1) KIT,MAXILLOFACIAL,PRESBYTERIAN, Catalog Number:PWV2MF104;  2) KIT,MAXILLOFACIAL,PRESBYTERIAN, Catalog Number:PWV2MF105  3) KIT,MAXILLOFACIAL,PRESBYTERIAN, Catalog Number:PWV2MF106  4) KIT,MAXILLOFACIAL,PRESBYTERIAN, Catalog Number:PWV2MF107  5) KIT,MAXILLOFACIAL,PRESBYTERIAN, Catalog Number:PWV2MF108  6) KIT,MAXILLOFACIAL,PRESBYTERIAN, Catalog Number:PWV2MF109  7) KIT,MAXILLOFACIAL,PRESBYTERIAN, Catalog Number:PWV2MF10V  8) KIT,MAXILLOFACIAL,PRESBYTERIAN, Catalog Number:PWV2MF10W  9) KIT,MAXILLOFACIAL,PRESBYTERIAN, Catalog Number:PWV2MF10Y  10) KIT,MAXILLOFACIAL,PRESBYTERIAN, Catalog Number:PWV2MF10Z  11) KIT,MAXILLOFACIAL,PRESBYTERIAN, Catalog Number:PWV2MF111  12) KIT,MAXILLOFACIAL,PRESBYTERIAN, Catalog Number:PWV2MF112  13) KIT,MAXILLOFACIAL,PRESBYTERIAN, Catalog Number:PWV2MFCP2  14) KIT,MAXILLOFACIAL PRESBYTERIAN, Catalog Number:PWV2MFCP3  15) KIT,MAXILLOFACIAL PRESBYTERIAN, Catalog Number:PWV2MFCP4  16) KIT,MAXILLOFACIAL,PRESBYTERIAN, Catalog N

## Reason for recall

Potential for 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-1130-2025
- **Recalling firm:** Cardinal Health 200, LLC
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2024-11-08
- **Report date:** 2025-02-19

- **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-1130-2025

## Citation

> AI Analytics. FDA recall Z-1130-2025. Retrieved 2026-08-12 from https://api.ai-analytics.org/recall/Z-1130-2025. Source: US FDA. Licensed CC0.

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