Device recall
Z-2166-2024: HORIBA custom configured fluorescence instrument, modular Fluorolog-QM
FDA device recall · Class II · Horiba Instruments Incorporated
Key facts
| Recall number (Z-number) | Z-2166-2024 |
|---|---|
| Recall event | 94839 |
| Product | HORIBA custom configured fluorescence instrument, modular Fluorolog-QM |
| Product code | REM |
| Recalling firm | Horiba Instruments Incorporated |
| Recall class | Class II |
| Status | Open, Classified |
| FEI number | 3014443691 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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