Dynex recalls Agility Sample Tips model 67910 due to incorrect labeling causing scanning errors. This prevents proper use with the Agility system and delays patient results.
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.
Dynex is recalling Agility Sample Tips with model number 67910 because the internal label is incorrectly labeled as reagent tip racks. This causes the tips to be misidentified by the Agility instrument, preventing proper use and delaying patient results.
The sample tips have an internal label that incorrectly identifies them as reagent tip racks instead of sample tip racks. When scanned by the Agility instrument, the system misidentifies the tips, making them incompatible and preventing proper use. This causes delays in obtaining patient results.
Users of the Dynex Agility Automated ELISA system who have the model 67910 sample tips may be affected. Those who use these tips for patient testing are most at risk of delayed results.
Check for the model number 67910 on the sample tips. The tips are used with the Agility Automated ELISA system and have a lot number of 863366.
Verify the internal label on the sample tip rack to ensure it is correctly labeled as sample tip racks, not reagent tip racks.
The internal label on the sample tip rack is incorrectly labeled as reagent tip racks, causing the Agility instrument to misidentify the tips and prevent proper use.
This recall causes delays in obtaining patient results because the tips are incompatible with the system and cannot be used properly.
Look for the model number 67910 on the sample tips, which are used with the Agility Automated ELISA system and have a lot number of 863366.
We’ve drafted a message you can send Dynex to request your refund or repair — edit it as you like.
Subject: Recall Z-2345-2025 — Dynex Dynex Hello, I own a Dynex that is covered by recall Z-2345-2025 from Dynex. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
