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...
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
About Dynex Technologies, Inc.
Dynex Technologies, Inc. has 2 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report