Device recall
Z-1384-2022: Kit Label: Anti-FITC-AP CISH Accessory Kit (Dako Omnis), Box A REF K589911-2…
FDA device recall · Class III · Agilent Technologies, Inc.
Key facts
| Recall number (Z-number) | Z-1384-2022 |
|---|---|
| Recall event | 90435 |
| Product | Kit Label: Anti-FITC-AP CISH Accessory Kit (Dako Omnis), Box A REF K589911-2 Anti-FITC-AP CISH Accessory Kit (Dako Omnis), Box A REF K589911-21 Vial Labels: Mat. No K589911-21512 |
| Product code | PPM |
| Recalling firm | Agilent Technologies, Inc. |
| Recall class | Class III |
| Status | Open, Classified |
| FEI number | 2916205 |
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