Device recall
Z-1843-2019: Aquarius D13S319 Plus Deletion Probe, Model LPH068-A Product Usage: The D13S319…
FDA device recall · Class III · Cytocell Ltd.
Key facts
| Recall number (Z-number) | Z-1843-2019 |
|---|---|
| Recall event | 82917 |
| Product | Aquarius D13S319 Plus Deletion Probe, Model LPH068-A Product Usage: The D13S319 probe, labelled in red, covers a 156kb region including most of the DLEU2 gene, part of the DLEU1 gene and the D13S319 and D13S272 markers. The 13qter subtelomere specific probe, labelled in green, allows identification… |
| Product code | MVU |
| Recalling firm | Cytocell Ltd. |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Jul 16, 2020 |
| FEI number | 3002646096 |
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