# FDA recall Z-0287-2024

> **Stryker Corporation** · Class II · device recall initiated 2023-09-13.

## Product

Stryker, REF: CAT00241, Portal Entry Kit consisting of a skin marker, disposable ruler, (2) FlexSticks, 30 ml syringe, and (2) 17 Ga Needles. Used to aid the surgeon in  establishing arthroscopic portals and joint access.

## Reason for recall

Expired product distributed

## Distribution

US: NH, TX, NY, NJ, OH, MN OUS: None

## Key facts

- **Recall number:** Z-0287-2024
- **Recalling firm:** Stryker Corporation
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2023-09-13
- **Report date:** 2023-11-15

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** San Jose, CA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0287-2024

## Citation

> AI Analytics. FDA recall Z-0287-2024. Retrieved 2026-07-13 from https://api.ai-analytics.org/recall/Z-0287-2024. Source: US FDA. Licensed CC0.

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