---
title: "Stryker, REF: CAT00241, Portal Entry Kit consisting of a skin marker, disposa... — FDA record Z-0287-2024 | Is It on Recall"
description: "Expired product distributed"
url: https://isitonrecall.com/recall/fda-device-z-0287-2024-stryker-ref-cat00241-portal-entry-kit-consisting-of-a-skin-marker-disposable-ruler-2-flexsticks-30-m/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

[Recall archive](https://isitonrecall.com/archives/) / FDA device enforcement

# Stryker, REF: CAT00241, Portal Entry Kit consisting of a skin marker, disposable ruler, (2) FlexSticks, 30 ml syringe... — FDA record Z-0287-2024

Reported ongoing

Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.

Source date Sep 13, 2023. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/).

## What the record says

- **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**: Expired product distributed
- **Classification**: Class II
- **Recalling firm**: Stryker Corporation
- **Quantity**: 19 kits
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-0287-2024

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0287-2024%22)

[What the recall classes mean](https://isitonrecall.com/guides/recall-classes/). Classification is an agency assessment, not individual medical advice.

## Lot and product identifiers

| Label field | Details supplied by the agency |
| --- | --- |
| Lot, code or applicability | Lot # 007047/UDI: 07613252632863 |

Match all identifying details in the current notice. A brand name alone is not enough.

## Distribution

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

States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.

- [Minnesota](https://isitonrecall.com/state/minnesota/)
- [New Hampshire](https://isitonrecall.com/state/new-hampshire/)
- [New Jersey](https://isitonrecall.com/state/new-jersey/)
- [New York](https://isitonrecall.com/state/new-york/)
- [Ohio](https://isitonrecall.com/state/ohio/)
- [Texas](https://isitonrecall.com/state/texas/)

## Dates in the source

- **Report date**: Nov 15, 2023
- **Recall initiation date**: Sep 13, 2023
- **Center classification date**: Nov 9, 2023

FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.

## What to do next

Read the official notice for the action that applies to your exact product.

[Read the current instructions](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0287-2024%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Stryker Corporation records](https://isitonrecall.com/brand/stryker-corporation/)