Device recall
Z-2140-2024: Life2000 Ventilator, Product Code: MS-01-0118, which is contained in the…
FDA device recall · Class I · Baxter Healthcare Corporation
Key facts
| Recall number (Z-number) | Z-2140-2024 |
|---|---|
| Recall event | 94701 |
| Product | Life2000 Ventilator, Product Code: MS-01-0118, which is contained in the Life2000 Ventilator System, with Product Codes BT-20-0002, BT-20-0002A and BT-20-0002AP. The Life2000 ventilation system includes the Life2000 ventilator which has its individual label. |
| Product code | CBK |
| Recalling firm | Baxter Healthcare Corporation |
| Recall class | Class I |
| Status | Open, Classified |
| 510(k) numbers | K170037 |
| FEI number | 1417572 |
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