Device recall
Z-1480-2018: Oncomine Dx Target Test, (Model No. A32451), Oncomine Dx Target RNA/DNA Panel…
FDA device recall · Class II · Life Technologies Corporation
Key facts
| Recall number (Z-number) | Z-1480-2018 |
|---|---|
| Recall event | 79649 |
| Product | Oncomine Dx Target Test, (Model No. A32451), Oncomine Dx Target RNA/DNA Panel (Model No. A32441). A qualitative In Vitro Diagnostic test. |
| Product code | PQP |
| Recalling firm | Life Technologies Corporation |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 12, 2020 |
| PMA numbers | P160045 |
| FEI number | 3003335080 |
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