Device recall
Z-1651-2022: therascreen FGFR RGQ RT-PCR Kit (CE IVD, not sold in the US) REF 874711
FDA device recall · Class II · Qiagen Sciences LLC
Key facts
| Recall number (Z-number) | Z-1651-2022 |
|---|---|
| Recall event | 90691 |
| Product | therascreen FGFR RGQ RT-PCR Kit (CE IVD, not sold in the US) REF 874711 |
| Product code | OWD |
| Recalling firm | Qiagen Sciences LLC |
| Recall class | Class II |
| Status | Open, Classified |
| PMA numbers | P180043 |
| FEI number | 3003572099 |
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