Drug recall
Dynex Agility Sample Tips; Model Number: 67910; The 67910 Agility Sample Tips are an accessory/consumable used…
FDA recall event 97319 · Class II · Dynex Technologies, Inc.
Key facts
| Event ID | 97319 |
|---|---|
| Recall numbers | Z-2345-2025 |
| Recalling firm | Dynex Technologies, Inc. |
| Product type | Devices |
| Products | Dynex Agility Sample Tips; Model Number: 67910; The 67910 Agility Sample Tips are an accessory/consumable used with the Agility Automated ELISA system. |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | 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… |
| Initiation date | Jul 16, 2025 |
| Report date | Aug 27, 2025 |
| City | Chantilly |
| State | VA |
| Country | United States |
| FEI number | 1117676 |
At a glance
- 1–9 Products in this recall
- 1–9 FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: