Device recall
Z-1139-2023: Life2000 Ventilator System, a) REF BT-20-0002, b) REF BT-20-0002A, ventilatory…
FDA device recall · Class I · Baxter Healthcare Corporation
Key facts
| Recall number (Z-number) | Z-1139-2023 |
|---|---|
| Recall event | 91506 |
| Product | Life2000 Ventilator System, a) REF BT-20-0002, b) REF BT-20-0002A, ventilatory support for the care of individuals |
| 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