---
title: "Guide Wire with Ruler Tube 3x1000 mm DIA; Catalog number/REF: 2351-3100S; — FDA record Z-1621-2025 | Is It on Recall"
description: "The metal ring at the end of the Guide Wire with Ruler Tube may detach from the main body of the instrument during use in surgery."
url: https://isitonrecall.com/recall/fda-device-z-1621-2025-guide-wire-with-ruler-tube-3x1000-mm-dia-catalog-number-ref-2351-3100s/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# Guide Wire with Ruler Tube 3x1000 mm DIA; Catalog number/REF: 2351-3100S; — FDA record Z-1621-2025

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 Mar 28, 2025. 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**: Guide Wire with Ruler Tube 3x1000 mm DIA; Catalog number/REF: 2351-3100S;
- **Reason**: The metal ring at the end of the Guide Wire with Ruler Tube may detach from the main body of the instrument during use in surgery.
- **Classification**: Class II
- **Recalling firm**: Stryker GmbH
- **Quantity**: 6407 units
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-1621-2025

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1621-2025%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 | Catalog number/REF: 2351-3100S; UDI-DI: 07613327361803; Lot #: KU164143, KU164755, KU164756, KU164757, KU164758, KU164759, KU164760, KU164761, KU164762, KU164763, KU164764, KU164765, KU164766, KU164767, KU164768, KU164769, KU164770, KU164771, KU164772, KU164773, KU164774, KU164775, KU164776, KU164777, KU164778, KU164779, KU164780, KU164781, KU164782, KU164783, KU164784, KU165161, KU165162, KU165163, KU165164, KU165165, KU165166, KU165167, KU165168, KU165169, KU165170, KU165171, KU165172, KU165173, KU165174, KU165175, KU184035, KU184036, KU184039, KU184041, KU184042, KU184044, KU184045, KU184046, KU184047, KU184049. |

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

## Distribution

US Nationwide distribution in the states of CA, GA, IL, KY, MA, MD, NY, OH, TN, TX, WV.

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

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## Dates in the source

- **Report date**: Apr 23, 2025
- **Recall initiation date**: Mar 28, 2025
- **Center classification date**: Apr 17, 2025

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-1621-2025%22)

## Related records

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