Device recall
Z-1202-2019: Aquarius CSF1R/RPS14 (5q32-q33) Probe Red, Model LPH540-A Analyte specific…
FDA device recall · Class III · Cytocell Ltd.
Key facts
| Recall number (Z-number) | Z-1202-2019 |
|---|---|
| Recall event | 82599 |
| Product | Aquarius CSF1R/RPS14 (5q32-q33) Probe Red, Model LPH540-A Analyte specific reagent. |
| Product code | MVU |
| Recalling firm | Cytocell Ltd. |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Oct 13, 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