---
title: "Dynex Agility Sample Tips; Model Number: 67910; The 67910 Agility Sample Tips... — FDA record Z-2345-2025 | Is It on Recall"
description: "The internal label affixed to the sample tip rack is incorrectly labeled as reagent tip racks. When scanned by the Agility instrument, the tip rack is misidenti"
url: https://isitonrecall.com/recall/fda-device-z-2345-2025-dynex-agility-sample-tips-model-number-67910-the-67910-agility-sample-tips-are-an-accessory-consumab/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# Dynex Agility Sample Tips; Model Number: 67910; The 67910 Agility Sample Tips are an accessory/consumable used with t... — FDA record Z-2345-2025

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 Jul 16, 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**: Dynex Agility Sample Tips; Model Number: 67910; The 67910 Agility Sample Tips are an accessory/consumable used with the Agility Automated ELISA system.
- **Reason**: The internal label affixed to the sample tip rack is incorrectly labeled as reagent tip racks. When scanned by the Agility instrument, the tip rack is misidentified as a different tip type, rendering it incompatible with the system and preventing use which causes a delay in obtaining patient results.
- **Classification**: Class II
- **Recalling firm**: Dynex Technologies, Inc.
- **Quantity**: 237 units
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-2345-2025

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2345-2025%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 | Model Number: 67910; UDI-DI: 5060456180072; Lot Number: 863366; |

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

## Distribution

Domestic: CA, FL, NC, NJ, NY;

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

- [California](https://isitonrecall.com/state/california/)
- [Florida](https://isitonrecall.com/state/florida/)
- [North Carolina](https://isitonrecall.com/state/north-carolina/)
- [New Jersey](https://isitonrecall.com/state/new-jersey/)
- [New York](https://isitonrecall.com/state/new-york/)

## Dates in the source

- **Report date**: Aug 27, 2025
- **Recall initiation date**: Jul 16, 2025
- **Center classification date**: Aug 21, 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-2345-2025%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Dynex Technologies, Inc. records](https://isitonrecall.com/brand/dynex-technologies-inc/)