Device recall
Z-2130-2024: ZOLL 731 Ventilator (EMV+, AEV, Eagle II) - for MRI Compatible Devices…
FDA device recall · Class I · ZOLL Medical Corporation
Key facts
| Recall number (Z-number) | Z-2130-2024 |
|---|---|
| Recall event | 94589 |
| Product | ZOLL 731 Ventilator (EMV+, AEV, Eagle II) - for MRI Compatible Devices - Operator's Guide and Quick Reference Guide (QRGs) as follows: Part Numbers: 1. 799-EGL2-02 2. 799-EGL2-02-01 3. 799-EGL2-02-04 4. 799-EGL2-02-05 5. 799-EGL2-02-08 6. 799-EGL2-02-10 7. 799-EGL2-02-11 8. 799-EGL2-02-15 9… |
| Product code | CBK |
| Recalling firm | ZOLL Medical Corporation |
| Recall class | Class I |
| Status | Open, Classified |
| 510(k) numbers | K111473, K162832 |
| FEI number | 1220908 |
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