Device recall
Z-0824-2022: Cytocell 8 Square Template Slides (Glass)- microscope slides Reference: PCN008
FDA device recall · Class III · Cytocell Ltd.
Key facts
| Recall number (Z-number) | Z-0824-2022 |
|---|---|
| Recall event | 89747 |
| Product | Cytocell 8 Square Template Slides (Glass)- microscope slides Reference: PCN008 |
| Product code | PPM |
| Recalling firm | Cytocell Ltd. |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Jun 12, 2023 |
| 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