Device recall
Z-1082-04: Pipette Sample Tip, Product part #65910, packaged in cardboard cartons…
FDA device recall · Class II · Dynex Technologies, Inc.
Key facts
| Recall number (Z-number) | Z-1082-04 |
|---|---|
| Recall event | 29421 |
| Product | Pipette Sample Tip, Product part #65910, packaged in cardboard cartons containing 4 plastic racks of 108 pipette tips per rack. Pipette tips are accessory component for Dynex Technologies proprietary automated DSX system. |
| Product code | JQW |
| Recalling firm | Dynex Technologies, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 18, 2004 |
| FEI number | 1117676 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 Recalled products with this product code
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device recalls (products)
Each recalled device product receives a Z-number. Recall details such as root cause, distribution and firm actions are available in Orca1.
Source: U.S. Food and Drug Administration (FDA), Medical Device Recalls database