Device recall
Z-1809-2015: Lifesaver Single Patient Use Manual Resuscitator Product Usage: The Hudson RCI…
FDA device recall · Class I · Teleflex Medical
Key facts
| Recall number (Z-number) | Z-1809-2015 |
|---|---|
| Recall event | 71254 |
| Product | Lifesaver Single Patient Use Manual Resuscitator Product Usage: The Hudson RCI Lifesaver Single Patient Use manual resuscitator with pressure monitoring port is a disposable medical device intended for use on patients requiring temporary augmentation of ventilation with or without supplemental… |
| Product code | BTM |
| Recalling firm | Teleflex Medical |
| Recall class | Class I |
| Status | Terminated |
| Termination date | May 13, 2024 |
| 510(k) numbers | K964719 |
| 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