Device recall
Z-0009-2020: Babi.Plus 12.5 cm H2O Pressure Relief Manifold Catalog # 2691 for use with…
FDA device recall · Class I · TELEFLEX-MORRISVILLE
Key facts
| Recall number (Z-number) | Z-0009-2020 |
|---|---|
| Recall event | 83119 |
| Product | Babi.Plus 12.5 cm H2O Pressure Relief Manifold Catalog # 2691 for use with ventilators. |
| Product code | BZD |
| Recalling firm | TELEFLEX-MORRISVILLE |
| Recall class | Class I |
| Status | Terminated |
| Termination date | Jun 12, 2024 |
| 510(k) numbers | K110383 |
| FEI number | 3005747797 |
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