Device recall
Z-0560-2019: Atrium 28Fr PVC Thoracic Catheter RIGHT ANGLE, Part No. 8128
FDA device recall · Class II · Atrium Medical Corporation
Key facts
| Recall number (Z-number) | Z-0560-2019 |
|---|---|
| Recall event | 81524 |
| Product | Atrium 28Fr PVC Thoracic Catheter RIGHT ANGLE, Part No. 8128 |
| Product code | GBZ |
| Recalling firm | Atrium Medical Corporation |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 12, 2020 |
| 510(k) numbers | K831931 |
| FEI number | 3011175548 |
At a glance
- 1–9 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