Device recall
Z-2670-2026: Radius VSM ECG pre-connected Set, REF: 4842, 4695
FDA device recall · Class II · Masimo Corporation
Key facts
| Recall number (Z-number) | Z-2670-2026 |
|---|---|
| Recall event | 98481 |
| Product | Radius VSM ECG pre-connected Set, REF: 4842, 4695 |
| Product code | MHX |
| Recalling firm | Masimo Corporation |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K223498 |
| FEI number | 3011353843 |
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