Device recall
Z-0913-2026: GE Healthcare Carestation anesthesia system, product number and REF numbers…
FDA device recall · Class I · GE Medical Systems China Co., Ltd.
Key facts
| Recall number (Z-number) | Z-0913-2026 |
|---|---|
| Recall event | 98064 |
| Product | GE Healthcare Carestation anesthesia system, product number and REF numbers: Carestation 610 A1, REF 1012-9620-222; Carestation 620 A1 REF 1012-9620-000; Carestation 620 A1, REF 1012-9620-200; Carestation 620 A1, REF 1012-9620-202; Carestation 620 SE A1, REF 1012-9620-212; Carestation 630 A1, REF… |
| Product code | BSZ |
| Recalling firm | GE Medical Systems China Co., Ltd. |
| Recall class | Class I |
| Status | Open, Classified |
| 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