Device recall
Z-1949-2026: Brand Name: Genius" Review Station Product Name: Genius" Review Station Display…
FDA device recall · Class II · Hologic, Inc
Key facts
| Recall number (Z-number) | Z-1949-2026 |
|---|---|
| Recall event | 98487 |
| Product | Brand Name: Genius" Review Station Product Name: Genius" Review Station Display (Barco Monitor) Model/Catalog Number: CMP-01669 Software Version: N/A - not software version specific Component: Yes, the Genius" Review Station is a component of the Genius" Digital Diagnostics System with the Genius"… |
| Product code | QYV |
| Recalling firm | Hologic, Inc |
| Recall class | Class II |
| Status | Open, Classified |
| FEI number | 1000120743 |
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