Device recall
Z-0163-2022: Pneupac paraPac plus 300 ventilator kit, REF P300NGB
FDA device recall · Class III · Smiths Medical ASD Inc.
Key facts
| Recall number (Z-number) | Z-0163-2022 |
|---|---|
| Recall event | 88675 |
| Product | Pneupac paraPac plus 300 ventilator kit, REF P300NGB |
| Product code | BTL |
| Recalling firm | Smiths Medical ASD Inc. |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Aug 11, 2023 |
| 510(k) numbers | K123957 |
| FEI number | 3012307300 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 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