Device recall
Z-3250-2026: ForeSight Elite Tissue Oximetry Cable REF HEMFSM10 UDI-DI code: 00690103210927…
FDA device recall · Class II · Becton, Dickinson and Company
Key facts
| Recall number (Z-number) | Z-3250-2026 |
|---|---|
| Recall event | 99370 |
| Product | ForeSight Elite Tissue Oximetry Cable REF HEMFSM10 UDI-DI code: 00690103210927 The non-invasive ForeSight oximeter cable is intended for use as an adjunct monitor of absolute regional hemoglobin oxygen saturation of blood under the sensors in individuals at risk for reduced flow or no flow ischemic… |
| Product code | MUD |
| Recalling firm | Becton, Dickinson and Company |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K243781 |
| FEI number | 3032916632 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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