Device recall
Z-1072-04: Gen-Probe Amplified Mycobacterium Tuberculosis Direct Test, Catalog number 1001,
FDA device recall · Class III · Gen Probe Inc
Key facts
| Recall number (Z-number) | Z-1072-04 |
|---|---|
| Recall event | 29380 |
| Product | Gen-Probe Amplified Mycobacterium Tuberculosis Direct Test, Catalog number 1001, |
| Product code | NDZ |
| Recalling firm | Gen Probe Inc |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Sep 9, 2004 |
| FEI number | 2024800 |
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