Device recall
Z-0639-2016: Mercury Medical Neo-Tee T-Piece Resuscitator and T-Piece Circuit. The Neo-Tee…
FDA device recall · Class II · Mercury Enterprises, Inc. dba Mercury Medical
Key facts
| Recall number (Z-number) | Z-0639-2016 |
|---|---|
| Recall event | 72540 |
| Product | Mercury Medical Neo-Tee T-Piece Resuscitator and T-Piece Circuit. The Neo-Tee T-Piece Resuscitator is a gas powered emergency resuscitator intended to provide emergency respiratory support by means of a face mask or a tube inserted into a patient's airway. It is intended for use with neonates and… |
| Product code | BTL |
| Recalling firm | Mercury Enterprises, Inc. dba Mercury Medical |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Oct 13, 2017 |
| 510(k) numbers | K093913 |
| FEI number | 1024404 |
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