Device recall
Z-0580-2018: Carestation 620 A2, Carestation 650 A2, and Carestation 650c A2
FDA device recall · Class II · GE Medical Systems China Co., Ltd.
Key facts
| Recall number (Z-number) | Z-0580-2018 |
|---|---|
| Recall event | 78469 |
| Product | Carestation 620 A2, Carestation 650 A2, and Carestation 650c A2 |
| Product code | BSZ |
| Recalling firm | GE Medical Systems China Co., Ltd. |
| Recall class | Class II |
| Status | Open, Classified |
| FEI number | 3003513129 |
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