Device recall
Z-0350-2020: Universal Sexual Health Testing Kit
FDA device recall · Class II · Privapath Diagnostics Ltd
Key facts
| Recall number (Z-number) | Z-0350-2020 |
|---|---|
| Recall event | 83709 |
| Product | Universal Sexual Health Testing Kit |
| Recalling firm | Privapath Diagnostics Ltd |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Nov 23, 2020 |
| FEI number | 3015209536 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 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