Device recall
Z-1358-2023: Agilent Resolution ctDx FIRST Sample Collection Kit, 500032
FDA device recall · Class III · AGILENT TECHNOLOGIES INC./US
Key facts
| Recall number (Z-number) | Z-1358-2023 |
|---|---|
| Recall event | 91863 |
| Product | Agilent Resolution ctDx FIRST Sample Collection Kit, 500032 |
| Product code | PQP |
| Recalling firm | AGILENT TECHNOLOGIES INC./US |
| Recall class | Class III |
| Status | Open, Classified |
| PMA numbers | P210040, P210040/A005, P210040/A006 |
| FEI number | 3019893001 |
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