# FDA recall Z-1136-2025

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

## Product

Cardinal Health Presource Kits:  1) OPHTHALMOLOGY ENDO DCR XTRS PK, Catalog Number:SEY30EYRVA;  2) OPHTHALMOLOGY ENDO DCR XTRS PK, Catalog Number:SEY30EYRVB  3) OPHTHALMOLOGY ENDO DCR XTRS PK, Catalog Number:SEY30EYRVC  4) OCULAR PLASTIC PACK, Catalog Number:SEY35OP961  5) OCULAR PLASTIC PACK, Catalog Number:SEY35OP962  6) OCULAR PLASTIC PACK, Catalog Number:SEY35OP96A  7) OCULAR PLASTIC PACK, Catalog Number:SEY35OP96B  8) OCULAR PLASTIC PACK, Catalog Number:SEY35OP96C  9) OCULAR PLASTIC PACK, Catalog Number:SEY35OPBLX  10) OCULAR PLASTIC PACK, Catalog Number:SEY35OPBLY  11) OCULAR PLASTIC PACK, Catalog Number:SEY35OPBLZ

## 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-1136-2025
- **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-1136-2025

## Citation

> AI Analytics. FDA recall Z-1136-2025. Retrieved 2026-08-17 from https://api.ai-analytics.org/recall/Z-1136-2025. Source: US FDA. Licensed CC0.

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