Device recall
Z-0253-2020: Port full Access Tray Product Code: DT19330
FDA device recall · Class II · Centurion Medical Products Corporation
Key facts
| Recall number (Z-number) | Z-0253-2020 |
|---|---|
| Recall event | 83542 |
| Product | Port full Access Tray Product Code: DT19330 |
| Product code | LRP |
| Recalling firm | Centurion Medical Products Corporation |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 31, 2020 |
| 510(k) numbers | K021999 |
| FEI number | 3008403546 |
At a glance
- 1–9 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