Device recall
Z-1280-2023: Scan Monitor/ScanWatch, model number hwa09 Wearable, Bluetooth-connected wrist…
FDA device recall · Class II · Withings
Key facts
| Recall number (Z-number) | Z-1280-2023 |
|---|---|
| Recall event | 91523 |
| Product | Scan Monitor/ScanWatch, model number hwa09 Wearable, Bluetooth-connected wrist watch that records heart activity (ECG) and oxygen saturation (SpO2) |
| Product code | DPS |
| Recalling firm | Withings |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K201456 |
| FEI number | 3008820594 |
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