Class II — Potential Health Hazard

Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.

Dynex Agility Sample Tips Recalled by Dynex Technologies, Inc. Due to The internal label affixed to the sample tip...

Date: July 16, 2025
Company: Dynex Technologies, Inc.
Status: Ongoing
Source: FDA (Device)

What You Should Do

Stop using this product immediately. Do not consume, use, or distribute it.

Return the product to the place of purchase for a full refund. If you have questions, contact Dynex Technologies, Inc. directly.

Affected Products

Dynex Agility Sample Tips; Model Number: 67910; The 67910 Agility Sample Tips are an accessory/consumable used with the Agility Automated ELISA system.

Quantity: 237 units

Why Was This Recalled?

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.

Where Was This Sold?

This product was distributed to 5 states: CA, FL, NJ, NY, NC

Affected (5 states)Not affected

About Dynex Technologies, Inc.

Dynex Technologies, Inc. has 2 total recalls tracked by RecallDetector.

Related Recalls

Data sourced from the FDA (Device). Last updated March 26, 2026. View original report