Device recall
Z-2954-2018: GE Carestation 620/650/650c, A1 and A2 (non-US distribution) anesthesia systems
FDA device recall · Class II · GE Medical Systems China Co., Ltd.
Key facts
| Recall number (Z-number) | Z-2954-2018 |
|---|---|
| Recall event | 80693 |
| Product | GE Carestation 620/650/650c, A1 and A2 (non-US distribution) anesthesia systems |
| Product code | BSZ |
| Recalling firm | GE Medical Systems China Co., Ltd. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Dec 16, 2020 |
| 510(k) numbers | K151570 |
| FEI number | 3003513129 |
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