# FDA recall Z-2943-2026

> **Cardinal Health 200, LLC** · Class II · device recall initiated 2026-07-14.

## Product

Cardinal Health Presource Kits:  1) HARMONIZED SPINE VCH PHC PACK , Catalog Number: SOP30SPBCC

## Reason for recall

Procedure kits contain MEDICOM Ritmed Neurological Sponges that were recalled due to unexpected variability in endotoxin levels.

## Distribution

US Nationwide. Canada.

## Key facts

- **Recall number:** Z-2943-2026
- **Recalling firm:** Cardinal Health 200, LLC
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2026-07-14
- **Report date:** 2026-08-19

- **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-2943-2026

## Citation

> MORVS. FDA recall Z-2943-2026. Retrieved 2026-10-18 from https://api.morvs.ai/recall/Z-2943-2026. Source: US FDA. Licensed CC0.

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