Device recall
Z-1936-2015: Ocean Water Seal Chest Drain, SINGLE W/AC P/N: 2002-100
FDA device recall · Class II · Atrium Medical Corporation
Key facts
| Recall number (Z-number) | Z-1936-2015 |
|---|---|
| Recall event | 71023 |
| Product | Ocean Water Seal Chest Drain, SINGLE W/AC P/N: 2002-100 |
| Product code | PAD |
| Recalling firm | Atrium Medical Corporation |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Apr 26, 2016 |
| 510(k) numbers | K043140, K043582, K081718 |
| 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