Device recall
Z-0457-2026: BATTERY FLEX-3S2P 10.8V 18650 LI-ION SMBUS used with affected patient monitors…
FDA device recall · Class II · GE Healthcare Finland Oy
Key facts
| Recall number (Z-number) | Z-0457-2026 |
|---|---|
| Recall event | 97786 |
| Product | BATTERY FLEX-3S2P 10.8V 18650 LI-ION SMBUS used with affected patient monitors Model No 2062895-001 Manufacturer Part Number U80296-1R01, revision S |
| Product code | MHX |
| Recalling firm | GE Healthcare Finland Oy |
| Recall class | Class II |
| Status | Open, Classified |
| FEI number | 3002806783 |
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